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1 substances in Reaxys
2016-05-04 15h:31m:12s (EST)
O O
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O
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Reaxys ID 1953349 View in Reaxys
1/1 CAS Registry Number: 33567-62-3 Chemical Name: 2-(2,5-dimethoxyphenyl)acetaldehyde; 2,5-dimethoxyphenyl acetaldehyde; 2,5-dimethoxyphenylacetaldehyde; 2-(2',5'-Dimethoxyphenyl)-ethanal; 2.5-Dimethoxyphenylacetaldehyd Linear Structure Formula: C10H12O3 Molecular Formula: C10H12O3 Molecular Weight: 180.203 Type of Substance: isocyclic InChI Key: LBMQTRYSDDYFCW-UHFFFAOYSA-N Note:
O O
O
Substance Label (9) Label References 12
Ren, Jing; Yang, Min; Liu, Hongchun; Cao, Danyan; Chen, Danqi; Li, Jian; Tang, Le; He, Jianhua; Chen, Yue-Lei; Geng, Meiyu; Xiong, Bing; Shen, Jingkang; Organic and Biomolecular Chemistry; vol. 13; nb. 5; (2015); p. 1531 - 1535, View in Reaxys
2i
Gualandi, Andrea; Canestrari, Pietro; Emer, Enrico; Cozzi, Pier Giorgio; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 528 - 536, View in Reaxys
25
Yoritate, Makoto; Meguro, Tatsuhiko; Matsuo, Naoya; Shirokane, Kenji; Sato, Takaaki; Chida, Noritaka; Chemistry - A European Journal; vol. 20; nb. 26; (2014); p. 8210 - 8216, View in Reaxys
1d
Maurin, Cedric; Bailly, Fabrice; Cotelle, Philippe; Tetrahedron; vol. 61; nb. 29; (2005); p. 7054 - 7058, View in Reaxys
13,R=H,Y=2,5OMe
Audia, James E.; Evrard, Deborah A.; Murdoch, Gwyn R.; Droste, James J.; Nissen, Jeffrey S.; Schenck, Kathy W.; Fludzinski, Pawel; Lucaites, Virginia L.; Nelson, David L.; Cohen, Marlene L.; Journal of Medicinal Chemistry; vol. 39; nb. 14; (1996); p. 2773 - 2780, View in Reaxys
23
Rosowsky, Andre; Mota, Clara E.; Wright, Joel E.; Freisheim, James H.; Heusner, James J.; et al.; Journal of Medicinal Chemistry; vol. 36; nb. 21; (1993); p. 3103 - 3112, View in Reaxys
6
Deshmukh, M. N.; Joshi, Shreerang V.; Synthetic Communications; vol. 18; nb. 13; (1988); p. 1483 - 1490, View in Reaxys
VI
Vig,O.P. et al.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 15B; (1977); p. 988 - 990, View in Reaxys
I, X=Y=OMe, n=1
Billman; Tonnis; Journal of pharmaceutical sciences; vol. 60; nb. 8; (1971); p. 1188 - 1192, View in Reaxys
Boiling Point (3) Boiling Point [°C]
Pressure (Boiling Point) [Torr]
References
122
1
Deshmukh, M. N.; Joshi, Shreerang V.; Synthetic Communications; vol. 18; nb. 13; (1988); p. 1483 - 1490, View in Reaxys
140 - 145
7-8
Vig,O.P. et al.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 15B; (1977); p. 988 - 990, View in Reaxys
112 - 113
0.7
Billman; Tonnis; Journal of pharmaceutical sciences; vol. 60; nb. 8; (1971); p. 1188 1192, View in Reaxys
NMR Spectroscopy (5) 1 of 5
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]
25
Frequency (NMR Spectroscopy) [MHz]
200
Location
supporting information
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Gualandi, Andrea; Canestrari, Pietro; Emer, Enrico; Cozzi, Pier Giorgio; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 528 - 536, View in Reaxys 2 of 5
Description (NMR Spec- Chemical shifts; Spectrum troscopy) Nucleus (NMR Spectroscopy)
13C
Solvents (NMR Spectro- chloroform-d1 scopy) Temperature (NMR Spectroscopy) [°C]
25
Frequency (NMR Spectroscopy) [MHz]
50
Location
supporting information
Gualandi, Andrea; Canestrari, Pietro; Emer, Enrico; Cozzi, Pier Giorgio; Advanced Synthesis and Catalysis; vol. 356; nb. 2-3; (2014); p. 528 - 536, View in Reaxys 3 of 5
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- chloroform-d1 scopy) Frequency (NMR Spectroscopy) [MHz]
300
Beierlein, Jennifer M.; Frey, Kathleen M.; Bolstad, David B.; Pelphrey, Phillip M.; Joska, Tammy M.; Smith, Adrienne E.; Priestley, Nigel D.; Wright, Dennis L.; Anderson, Amy C.; Journal of Medicinal Chemistry; vol. 51; nb. 23; (2008); p. 7532 - 7540, View in Reaxys 4 of 5
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Solvents (NMR Spectro- CDCl3 scopy) Deshmukh, M. N.; Joshi, Shreerang V.; Synthetic Communications; vol. 18; nb. 13; (1988); p. 1483 - 1490, View in Reaxys; Rosowsky, Andre; Mota, Clara E.; Wright, Joel E.; Freisheim, James H.; Heusner, James J.; et al.; Journal of Medicinal Chemistry; vol. 36; nb. 21; (1993); p. 3103 - 3112, View in Reaxys 5 of 5
Description (NMR Spec- Chemical shifts troscopy) Nucleus (NMR Spectroscopy)
1H
Vig,O.P. et al.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 15B; (1977); p. 988 - 990, View in Reaxys IR Spectroscopy (3) 1 of 3
Description (IR Spectroscopy)
Bands
Solvent (IR Spectroscopy)
neat (no solvent)
Comment (IR Spectroscopy)
3000 - 1730 cm**(-1)
Rosowsky, Andre; Mota, Clara E.; Wright, Joel E.; Freisheim, James H.; Heusner, James J.; et al.; Journal of Medicinal Chemistry; vol. 36; nb. 21; (1993); p. 3103 - 3112, View in Reaxys 2 of 3
Description (IR Spectroscopy)
Bands
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Solvent (IR Spectroscopy)
neat (no solvent)
Comment (IR Spectroscopy)
1720 cm**(-1)
Deshmukh, M. N.; Joshi, Shreerang V.; Synthetic Communications; vol. 18; nb. 13; (1988); p. 1483 - 1490, View in Reaxys 3 of 3
Description (IR Spectroscopy)
Bands
Vig,O.P. et al.; Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry; vol. 15B; (1977); p. 988 - 990, View in Reaxys; Billman; Tonnis; Journal of pharmaceutical sciences; vol. 60; nb. 8; (1971); p. 1188 - 1192, 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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