2-(2-Nitroprop-1-en-1-yl)naphthalene [1-(2-Naphthyl)-2-nitropropene]

Page 1

Reaxys

PubChem

eMolecules

Reactions (27)

Substances (3)

Structure

Citations (19)

Structure/Compound Data Chemical Name: 1-(β-naphthyl)-2-nitro-1-propene Reaxys Registry Number: 2558504

CAS Registry Number: 59832-12-1 Type of Substance: isocyclic Molecular Formula: C13H11NO2

Linear Structure Formula: C13H11NO2

Molecular Weight: 213.236 InChI Key: DTZVIBZSHDZFPP-UHFFFAOYSA-N

1

N° of preparations All Preps | All Reactions

Available Data

N° of ref.

2 prep out of 16 reactions.

Identification Physical Data (6) Spectra (3)

13

Synthesize | Hide Details Find similar Chemical Names and Synonyms 1-(β-naphthyl)-2-nitro-1-propene, 2-(2-nitro-1-propenyl)naphthalene, 1-(2-naphthyl)-2-nitropropene, 7-β-Nitropropenyl-1,2,3,4-tetrahydronaphthalin, 1-<2>Naphthyl-2-nitro-prop-1-en, 2-<2-Nitro-propenyl>-naphthalin Identification Substance Label (8) Label

Reference

2d

Meninno, Sara; Volpe, Chiara; Sala, Giorgio Della; Capobianco, Amedeo; Lattanzi, Alessandra

Beilstein Journal of Organic Chemistry, 2016 , vol. 12, p. 643 - 647 Title/Abstract Full Text View citing articles Show Details

2m

Wang, Tao; Shao, Ailong; Feng, Haiyan; Yang, Shuwu; Gao, Meng; Tian, Jun; Lei, Aiwen

Tetrahedron, 2015 , vol. 71, # 26-27 p. 4473 - 4477 Title/Abstract Full Text View citing articles Show Details


1e

Cai, Zhihua; Liu, Guodu; Jiao, Guangjun; Senanayake, Chris H.; Tang, Wenjun

Synthesis (Germany), 2013 , vol. 45, # 24 art. no. SS-2013-H0581-OP, p. 3355 - 3360 Title/Abstract Full Text View citing articles Show Details

13k

Ono, Noboru; Kawamura, Hisayuki; Bougauchi, Masahiro; Maruyama, Kazuhiro

Tetrahedron, 1990 , vol. 46, # 21 p. 7483 - 7496 Title/Abstract Full Text View citing articles Show Details

1k

Ono, Noboru; Kawamura, Hisayuki; Bougauchi, Masahiro; Maruyama, Kazuhiro

Journal of the Chemical Society, Chemical Communications, 1989 , # 20 p. 1580 - 1581 Title/Abstract Full Text View citing articles Show Details

6b

Foucaud, Andre; Razorilalana-Rabearivony, Claudia; Loukakou, Emile; Person, Herve

Journal of Organic Chemistry, 1983 , vol. 48, # 21 p. 3639 - 3644 Title/Abstract Full Text View citing articles Show Details

Tabelle XXII

Silver,R.F. et al.

Canadian Journal of Chemistry, 1967 , vol. 45, p. 1001 - 1006 Full Text View citing articles Show Details

Tabelle XIV

Currie,D.J. et al.

Canadian Journal of Chemistry, 1967 , vol. 45, p. 1567 - 1580 Full Text View citing articles Show Details

Physical Data Melting Point (3) Melting Point

Solvent (Melting Point)

Crystallizes With

81 83.5 °C

methanol

Reference Vilches-Herrera, Marcelo; Miranda-Sepulveda, Juan; Rebolledo-Fuentes, Marco; Fierro, Angelica; Luehr, Susan; Iturriaga-Vasquez, Patricio; Cassels, Bruce K.; Reyes-Parada, Miguel

Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 6 p. 2452 - 2460 Title/Abstract Full Text View citing articles Show Details

96 °C

diethyl ether

Foucaud, Andre; Razorilalana-Rabearivony, Claudia; Loukakou, Emile; Person, Herve

Journal of Organic Chemistry, 1983 , vol. 48, # 21 p. 3639 - 3644 Title/Abstract Full Text View citing articles Show Details

97 98 °C

ethanol

Silver,R.F. et al.

Canadian Journal of Chemistry, 1967 , vol. 45, p. 1001 - 1006 Full Text View citing articles Show Details

Crystal Property Description (1) Colour & Other Properties yellow

Reference Vilches-Herrera, Marcelo; Miranda-Sepulveda, Juan; Rebolledo-Fuentes, Marco; Fierro, Angelica; Luehr, Susan; Iturriaga-Vasquez, Patricio; Cassels, Bruce K.; Reyes-Parada, Miguel

Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 6 p. 2452 - 2460 Title/Abstract Full Text View citing articles Show Details

Further Information (1) Description (Further Information)

Reference

Further information

Currie,D.J. et al.

Canadian Journal of Chemistry, 1967 , vol. 45, p. 1567 - 1580 Full Text View citing articles Show Details

Liquid/Liquid Systems (MCS) (1) Description (Liquid/Liquid Systems (MCS))

Partner (Liquid/Liquid Systems (MCS))

Temperature (Liquid/Liquid Systems (MCS))

Distribution between solvent 1 + 2

cyclohexane; H2O

25 °C

Spectra

Reference Currie,D.J. et al.

Canadian Journal of Chemistry, 1966 , vol. 44, p. 1035 - 1043 Full Text View citing articles Show Details


NMR Spectroscopy (2) Description (NMR Spectroscopy)

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

Chemical shifts

1H

chloroform-d1

Vilches-Herrera, Marcelo; Miranda-Sepulveda, Juan; Rebolledo-Fuentes, Marco; Fierro, Angelica; Luehr, Susan; Iturriaga-Vasquez, Patricio; Cassels, Bruce K.; Reyes-Parada, Miguel

Bioorganic and Medicinal Chemistry, 2009 , vol. 17, # 6 p. 2452 - 2460 Title/Abstract Full Text View citing articles Show Details

Chemical shifts

1H

CDCl3

Foucaud, Andre; Razorilalana-Rabearivony, Claudia; Loukakou, Emile; Person, Herve

Journal of Organic Chemistry, 1983 , vol. 48, # 21 p. 3639 - 3644 Title/Abstract Full Text View citing articles Show Details

Rothman, Richard B.; Blough, Bruce E.; Woolverton, William L.; Anderson, Karen G.; Negus, S. Stevens; Mello, Nancy K.; Roth, Bryan L.; Baumann, Michael H.

Journal of Pharmacology and Experimental Therapeutics, 2005 , vol. 313, # 3 p. 1361 - 1369 Title/Abstract Full Text View citing articles Show Details

Reference

UV/VIS Spectroscopy (1) Description (UV/VIS Spectroscopy)

Reference

Absorption maxima

Currie,D.J. et al.

Canadian Journal of Chemistry, 1967 , vol. 45, p. 1567 - 1580 Full Text View citing articles Show Details

Chemical Name: (E)-2-(2-nitroprop-1-en-1-yl)naphthalene Reaxys Registry Number: 2450474

CAS Registry Number: 37629-58-6 Type of Substance: isocyclic Molecular Formula: C13H11NO2

Linear Structure Formula: C13H11NO2

Molecular Weight: 213.236 InChI Key: DTZVIBZSHDZFPP-CSKARUKUSA-N

2

Synthesize | Hide Details Find similar Chemical Names and Synonyms (E)-2-(2-nitroprop-1-en-1-yl)naphthalene, β-Methyl-β-nitro-2-naphthylethylen Identification Substance Label (4) Label

Reference

1j

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

1m

Li, Shengkun; Huang, Kexuan; Zhang, Xumu

Chemical Communications, 2014 , vol. 50, # 64 p. 8878 - 8881 Title/Abstract Full Text View citing articles Show Details

2m

Liu, Guodu; Liu, Xiangqian; Cai, Zhihua; Jiao, Guangjun; Xu, Guangqing; Tang, Wenjun

Angewandte Chemie - International Edition, 2013 , vol. 52, # 15 p. 4235 - 4238 Angew. Chem., 2013 , vol. 125, # 15 p. 4329 - 4332,4 Title/Abstract Full Text View citing articles Show Details

18

Dore,J.-C.; Viel,C.

Chimica Therapeutica, 1972 , vol. 7, p. 214 - 220 Full Text View citing articles Show Details

Physical Data

1 prep out of 9 reactions.

Identification Physical Data (3) Spectra (6)

5


Melting Point (2) Melting Point

Solvent (Melting Point)

Location

Reference

94 - 97 °C

methanol

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

86 °C

methanol

Dore,J.-C.; Viel,C.

Chimica Therapeutica, 1972 , vol. 7, p. 214 - 220 Full Text View citing articles Show Details

Crystal Property Description (1) Colour & Other Properties

Location

Reference

yellow

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

Spectra NMR Spectroscopy (4) Description (NMR Spectroscopy)

Nucleus (NMR Spectroscopy)

Solvents (NMR Spectroscopy)

Temperature (NMR Spectroscopy)

Frequency (NMR Spectroscopy)

Chemical shifts

1H

chloroform-d1

30 °C

Chemical shifts

13C

chloroform-d1

Chemical shifts Spectrum

1H

Chemical shifts Spectrum

13C

Location

Reference

300 MHz

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

30 °C

75 MHz

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

chloroform-d1

29.54 °C

400 MHz

supporting information

Li, Shengkun; Huang, Kexuan; Zhang, Xumu

Chemical Communications, 2014 , vol. 50, # 64 p. 8878 - 8881 Title/Abstract Full Text View citing articles Show Details

chloroform-d1

30.64 °C

100 MHz

supporting information

Li, Shengkun; Huang, Kexuan; Zhang, Xumu

Chemical Communications, 2014 , vol. 50, # 64 p. 8878 - 8881 Title/Abstract Full Text View citing articles Show Details

IR Spectroscopy (1) Description (IR Spectroscopy)

Solvent (IR Spectroscopy)

Location

Reference

Bands

potassium bromide

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

Mass Spectrometry (1) Description (Mass Spectrometry)

Location

Reference

electron impact (EI) time-of-flight mass spectra (TOFMS) spectrum

supporting information

Vidal-Albalat; Świderek; Izquierdo; Rodríguez; Moliner; González

Chemical Communications, 2016 , vol. 52, # 65 p. 10060 - 10063 Title/Abstract Full Text View citing articles Show Details

Reaxys Registry Number: 8618548

Type of Substance: isocyclic Molecular Formula: C13H11NO2

Linear Structure Formula: C13H11NO2

0 prep out of 2 reactions.

Identification

1


Molecular Weight: 213.236 InChI Key: DTZVIBZSHDZFPP-NTMALXAHSA-N

3

Synthesize | Hide Details Find similar

Identification Substance Label (1) Label

Reference

1e

Yadav; Subba Reddy; Srinivas; Ramalingam

Synlett, 2000 , # 10 p. 1447 - 1449 Title/Abstract Full Text View citing articles Show Details


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