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8 substances in Re2016-03-23 10h:27m:53s (EST) axys
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Reaxys ID 21694831 View in Reaxys
1/8 CAS Registry Number: 687603-66-3 Chemical Name: rac-3,4-methylenedioxypyrovalerone; 3,4MDPV; rac-MDPV; MDPV; rac-1-(benzo[d][1,3]dioxol-5-yl)-2(pyrrolidin-1-yl)pentan-1-one; 3,4-methylenedioxypyrovalerone Linear Structure Formula: C16H21NO3 Molecular Formula: C16H21NO3 Molecular Weight: 275.348 InChI Key: SYHGEUNFJIGTRX-UHFFFAOYSA-N Note:
O O O
N
Substance Label (1) Label References MDPV
Marusich, Julie A.; Antonazzo, Kateland R.; Wiley, Jenny L.; Blough, Bruce E.; Partilla, John S.; Baumann, Michael H.; Neuropharmacology; vol. 87; (2014); p. 206 - 213, View in Reaxys; Harvey, Eric L.; Baker, Lisa E.; Psychopharmacology; vol. 233; nb. 4; (2016); p. 673 - 680, View in Reaxys
Crystal Property Description (1) Colour & Other References Properties yellow-red
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
NMR Spectroscopy (1) 1 of 1
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]
500.1
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Mass Spectrometry (6) Description (Mass References Spectrometry) high resolution Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; mass spectrome- (2015); p. 287 - 293, View in Reaxys try (HRMS); electrospray ionisation (ESI); spectrum time-of-flight Sysoev, Alexey A.; Poteshin, Sergey S.; Chernyshev, Denis M.; Karpov, Alexander V.; Tuzkov, Yuriy B.; mass spectra Kyzmin, Vyacheslav V.; Sysoev, Alexander A.; European Journal of Mass Spectrometry; vol. 20; nb. 2; (TOFMS); electro- (2014); p. 185 - 192, View in Reaxys spray ionisation (ESI); APCI (atmospheric pressure chemical ionization); spectrum IT (ion trap); elec- Vircks, Kyle E.; Mulligan, Christopher C.; Rapid Communications in Mass Spectrometry; vol. 26; nb. 23; trospray ionisation (2012); p. 2665 - 2672, View in Reaxys (ESI); tandem mass spectrometry; CID (collisioninduced dissociation); fragmentation pattern; spectrum EI (Electron impact); Spectrum
Meyer, Markus R.; Du, Peng; Schuster, Frank; Maurer, Hans H.; Journal of Mass Spectrometry; vol. 45; nb. 12; (2010); p. 1426 - 1442, View in Reaxys
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LCMS (Liquid chromatography mass spectrometry); ESI (Electrospray ionisation); TOFMS (Time of flight mass spectrum); Spectrum
Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys
GCMS (Gas chro- Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications matography mass in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys spectrometry); EI (Electron impact); TOFMS (Time of flight mass spectrum); Spectrum Pharmacological Data (10) 1 of 10
Comment (Pharmacological Data)
Bioactivities present
Meyer, Markus R.; Du, Peng; Schuster, Frank; Maurer, Hans H.; Journal of Mass Spectrometry; vol. 45; nb. 12; (2010); p. 1426 - 1442, View in Reaxys; Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys; Vircks, Kyle E.; Mulligan, Christopher C.; Rapid Communications in Mass Spectrometry; vol. 26; nb. 23; (2012); p. 2665 - 2672, View in Reaxys; Sysoev, Alexey A.; Poteshin, Sergey S.; Chernyshev, Denis M.; Karpov, Alexander V.; Tuzkov, Yuriy B.; Kyzmin, Vyacheslav V.; Sysoev, Alexander A.; European Journal of Mass Spectrometry; vol. 20; nb. 2; (2014); p. 185 - 192, View in Reaxys; Marusich, Julie A.; Antonazzo, Kateland R.; Wiley, Jenny L.; Blough, Bruce E.; Partilla, John S.; Baumann, Michael H.; Neuropharmacology; vol. 87; (2014); p. 206 - 213, View in Reaxys; Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys; Patent; Randox Laboratories Ltd.; Benchik, Elouard; Fitzgerald, Peter; Lowry, Philip; McConnell, Ivan; EP2950104; (2015); (A1) English, View in Reaxys; Harvey, Eric L.; Baker, Lisa E.; Psychopharmacology; vol. 233; nb. 4; (2016); p. 673 - 680, View in Reaxys 2 of 10
Comment (Pharmacological Data)
physiological behaviour discussed
Harvey, Eric L.; Baker, Lisa E.; Psychopharmacology; vol. 233; nb. 4; (2016); p. 673 - 680, View in Reaxys 3 of 10
Comment (Pharmacological Data)
physiological behaviour discussed
Patent; Randox Laboratories Ltd.; Benchik, Elouard; Fitzgerald, Peter; Lowry, Philip; McConnell, Ivan; EP2950104; (2015); (A1) English, View in Reaxys 4 of 10
Comment (Pharmacological Data)
physiological behaviour discussed
Marusich, Julie A.; Antonazzo, Kateland R.; Wiley, Jenny L.; Blough, Bruce E.; Partilla, John S.; Baumann, Michael H.; Neuropharmacology; vol. 87; (2014); p. 206 - 213, View in Reaxys 5 of 10
Effect (Pharmacological Data)
biotransformation
Species or Test-System (Pharmacological Data)
urine of Wistar rat
Sex
male
Route of Application
intragastric
Concentration (Pharmacological Data)
20 mg/kg
Results
further metabolites given
Metabolite XRN (Pharmacological Data)
21694837; 10359927; 21694862; 21694864; 21694834; 21694843; 21694845; 21694844; 21694839
Metabolite (Pharmacological Data)
C16H19NO4; catechol PV; C22H31NO9; C22H29NO10; C16H23NO4; C16H21NO6; C16H21NO6; C16H19NO6; C15H21NO4
Meyer, Markus R.; Du, Peng; Schuster, Frank; Maurer, Hans H.; Journal of Mass Spectrometry; vol. 45; nb. 12; (2010); p. 1426 - 1442, View in Reaxys
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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6 of 10
Effect (Pharmacological Data)
biotransformation
Species or Test-System (Pharmacological Data)
urine of human
Results
further metabolites given
Metabolite XRN (Pharmacological Data)
21694837; 10359927; 21694862; 21694864; 21694839; 21694841; 21694836; 21694844; 21694830; 21694829
Metabolite (Pharmacological Data)
C16H19NO4; catechol PV; C22H31NO9; C22H29NO10; C15H21NO4; C16H23NO4; C16H23NO4; C16H19NO6; C12H17NO3; C11H15NO3
Meyer, Markus R.; Du, Peng; Schuster, Frank; Maurer, Hans H.; Journal of Mass Spectrometry; vol. 45; nb. 12; (2010); p. 1426 - 1442, View in Reaxys 7 of 10
Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
liver S9 cellular fractions of human
Further Details (Pharma- title comp. concentration not explicitly stated by authors; GC/MS cological Data) Type (Pharmacological Data)
unmetabolised title compound
Value of Type (Pharmacological Data)
80 percent
Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys 8 of 10
Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
liver S9 cellular fractions of human
Further Details (Pharma- title comp. concentration not explicitly stated by authors; GC/MS cological Data) Type (Pharmacological Data)
catechol formation rate
Value of Type (Pharmacological Data)
7 percent
Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys 9 of 10
Effect (Pharmacological Data)
pharmacokinetics
Species or Test-System (Pharmacological Data)
liver S9 cellular fractions of human
Further Details (Pharma- title comp. concentration not explicitly stated by authors; GC/MS cological Data) Type (Pharmacological Data)
methyl catechol formation rate
Value of Type (Pharmacological Data)
10 percent
Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys 10 of 10
Effect (Pharmacological Data)
biotransformation
Species or Test-System (Pharmacological Data)
liver S9 cellular fractions of human
Further Details (Pharma- title comp. concentration not explicitly stated by authors; GC/MS cological Data)
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Metabolite XRN (Pharmacological Data)
10359927; 21694832
Metabolite (Pharmacological Data)
catechol PV; methyl catechol PV
Strano-Rossi, Sabina; Cadwallader, Amy B.; de la Torre, Xavier; Botre, Francesco; Rapid Communications in Mass Spectrometry; vol. 24; nb. 18; (2010); p. 2706 - 2714, View in Reaxys
Reaxys ID 26499448 View in Reaxys
2/8 CAS Registry Number: 24622-62-6 Chemical Name: rac-3,4-methylenedioxypyrovalerone hydrochloride; MDPV; rac-1-(benzo[d][1,3]dioxol-5-yl)-2-(pyrrolidin-1yl)pentan-1-one hydrochloride; 3,4-methylenedioxypyrovalerone hydrochloride Linear Structure Formula: C16H21NO3*ClH Molecular Formula: C16H21NO3*ClH Molecular Weight: 311.809 InChI Key: PYQZNWFQAMFAMT-UHFFFAOYSA-N Note:
O O
HCl O N
Substance Label (2) Label References 4
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
6
Kolanos, Renata; Solis, Ernesto; Sakloth, Farhana; De Felice, Louis J.; Glennon, Richard A.; ACS Chemical Neuroscience; vol. 4; nb. 12; (2013); p. 1524 - 1529, View in Reaxys
Melting Point (1) 1 of 1
Melting Point [°C]
247 - 249
Comment (Melting Point) with decomposition Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Crystal Property Description (1) Colour & Other References Properties white
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
NMR Spectroscopy (2) 1 of 2
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]
400
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys 2 of 2
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- chloroform-d1 scopy)
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Frequency (NMR Spectroscopy) [MHz]
100
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Pharmacological Data (3) 1 of 3
Comment (Pharmacological Data)
Bioactivities present
Kolanos, Renata; Solis, Ernesto; Sakloth, Farhana; De Felice, Louis J.; Glennon, Richard A.; ACS Chemical Neuroscience; vol. 4; nb. 12; (2013); p. 1524 - 1529, View in Reaxys; King, Heather E.; Wetzell, Bradley; Rice, Kenner C.; Riley, Anthony L.; Pharmacology Biochemistry and Behavior; vol. 126; (2014); p. 163 - 169, View in Reaxys; Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys 2 of 3
Comment (Pharmacological Data)
physiological behaviour discussed
King, Heather E.; Wetzell, Bradley; Rice, Kenner C.; Riley, Anthony L.; Pharmacology Biochemistry and Behavior; vol. 126; (2014); p. 163 - 169, View in Reaxys 3 of 3
Comment (Pharmacological Data)
physiological behaviour discussed
Kolanos, Renata; Solis, Ernesto; Sakloth, Farhana; De Felice, Louis J.; Glennon, Richard A.; ACS Chemical Neuroscience; vol. 4; nb. 12; (2013); p. 1524 - 1529, View in Reaxys
Reaxys ID 28017714 View in Reaxys
3/8 Chemical Name: S-(-)-MDPV*(+)-BTA Linear Structure Formula: C16H21NO3*C10H10BrNO5 Molecular Formula: C10H10BrNO5*C16H21NO3 Molecular Weight: 579.445 InChI Key: GPDIYEZKUKYESU-FTGFJPOGSA-N Note:
Br
O
O HO N H OH
N O
HO O
O
Substance Label (1) Label References 5
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Melting Point (1) 1 of 1
Melting Point [°C]
130 - 132
Solvent (Melting Point)
acetone; diethyl ether
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Density (1) 1 of 1
Density [g·cm-3]
1.488
Measurement Tempera- -123.16 ture [°C] Type (Density)
crystallographic
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Crystal Phase (2) Description (Crys- Location tal Phase)
References
Structure of the solid
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
supporting information
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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Crystal growth
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Crystal Property Description (1) Colour & Other References Properties white
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Crystal System (1) Crystal System Location Rhombic
References
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Interatomic Distances and Angles (1) Description Location Comment (Interatomic Distances and Angles) Interatomic dissupporting infortances and angles mation
Single Crystal Xray Diffraction
References
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Optical Rotatory Power (1) 1 of 1
Type (Optical Rotatory Power)
[alpha]
Concentration (Optical Rotatory Power)
0.89 g/100ml
Solvent (Optical Rotatory Power)
methanol
Optical Rotatory Power [deg]
57.5
Wavelength (Optical Ro- 589 tatory Power) [nm] Temperature (Optical Rotatory Power) [°C]
23
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys Space Group (1) Space Group 19
Location
Comment (Space Group)
References
supporting information
a = 9.3654 Å; b = Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; 9.837 Å; c = Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, 28.0706 Å; Z = 4; View in Reaxys T = 150 K; Method = Single crystal Xray diffraction; atomic positions available
Reaxys ID 28017715 View in Reaxys
4/8 Chemical Name: R-(+)-MDPV*(-)-BTA Linear Structure Formula: C16H21NO3*C10H10BrNO5 Molecular Formula: C10H10BrNO5*C16H21NO3 Molecular Weight: 579.445 InChI Key: GPDIYEZKUKYESU-JGMGIOCMSA-N Note:
Br
O
O HO N H OH
N O
HO O
O
Substance Label (1) Label References
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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6
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Reaxys ID 28017716 View in Reaxys
5/8 Chemical Name: (S)-(-)-3,4-methylenedioxypyrovalerone; (S)(-)-MDPV; (S)-(-)-1-(benzo[d][1,3]dioxol-5-yl)-2-(pyrrolidin-1yl)pentan-1-one Linear Structure Formula: C16H21NO3 Molecular Formula: C16H21NO3 Molecular Weight: 275.348 InChI Key: SYHGEUNFJIGTRX-ZDUSSCGKSA-N Note:
O
N O O
Chromatographic Data (1) Chromatographic References data HPLC (High performance liquid chromatography)
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Optical Rotatory Power (1) 1 of 1
Type (Optical Rotatory Power)
[alpha]
Concentration (Optical Rotatory Power)
0.89 g/100ml
Enantiomeric excess [%ee]
98
Solvent (Optical Rotatory Power)
chloroform
Optical Rotatory Power [deg]
-6.5
Wavelength (Optical Ro- 589 tatory Power) [nm] Temperature (Optical Rotatory Power) [°C]
23
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys NMR Spectroscopy (1) 1 of 1
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Reaxys ID 28017717 View in Reaxys
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6/8
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Chemical Name: (R)-(+)-3,4-methylenedioxypyrovalerone; (R)(+)-MDPV; (R)-(+)-1-(benzo[d][1,3]dioxol-5-yl)-2-(pyrrolidin-1yl)pentan-1-one Linear Structure Formula: C16H21NO3 Molecular Formula: C16H21NO3 Molecular Weight: 275.348 InChI Key: SYHGEUNFJIGTRX-CYBMUJFWSA-N Note:
O
N O O
Chromatographic Data (1) Chromatographic References data HPLC (High performance liquid chromatography)
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
NMR Spectroscopy (1) 1 of 1
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Reaxys ID 28017718 View in Reaxys
7/8 Linear Structure Formula: C16H21NO3*ClH Molecular Formula: C16H21NO3*ClH Molecular Weight: 311.809 InChI Key: PYQZNWFQAMFAMT-ZOWNYOTGSA-N Note:
O
N O O HCl
NMR Spectroscopy (1) 1 of 1
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Reaxys ID 28017719 View in Reaxys
8/8 Linear Structure Formula: C16H21NO3*ClH Molecular Formula: C16H21NO3*ClH Molecular Weight: 311.809 InChI Key: PYQZNWFQAMFAMT-BTQNPOSSSA-N Note:
O
N
HCl
O O
NMR Spectroscopy (1) 1 of 1
Description (NMR Spec- Chemical shifts; Spectrum troscopy)
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Nucleus (NMR Spectroscopy)
1H
Location
supporting information
Suzuki, Masaki; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C.; Chirality; vol. 27; nb. 4; (2015); p. 287 - 293, View in Reaxys
Copyright © 2016 Reed Elsevier Properties SA. All rights reserved. Authorized use only. Reaxys® and the Reaxys® trademark are owned and protected by Reed Elsevier Properties SA and used under license.
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