42288-26-6

42288-26-6 structure

Name: N-(4-Cyanophenyl)glycine
Chemical Name: 2-((4-Cyanophenyl)amino)acetic acid
CAS Number: 42288-26-6
Molecular Formula: C₉H₈N₂O₂
Molecular Weight: 176.172
Catalog: Research Areas Others
Create Date: 2018-07-16 18:04:14
Modify Date: 2024-01-02 12:20:17
N-(4-Cyanophenyl)glycine is a Glycine (HY-Y0966) derivative[1].

Name	2-((4-Cyanophenyl)amino)acetic acid
Synonyms	N-(4-Cyano-Phenyl)-Glycine Glycine, N-(4-cyanophenyl)- N-(4-Cyanophenyl)glycine 2-(4-Cyanophenylamino)acetic acid N-(4-Cyanophenyl)-glycine

Description	N-(4-Cyanophenyl)glycine is a Glycine (HY-Y0966) derivative[1].
Related Catalog	Research Areas >> Others Signaling Pathways >> Others >> Others
In Vitro	Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References	[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Density	1.3±0.1 g/cm3
Boiling Point	447.2±30.0 °C at 760 mmHg
Melting Point	237 °C(dec.)
Molecular Formula	C₉H₈N₂O₂
Molecular Weight	176.172
Flash Point	224.3±24.6 °C
Exact Mass	176.058578
PSA	73.12000
LogP	0.55
Vapour Pressure	0.0±1.1 mmHg at 25°C
Index of Refraction	1.594

Hazard Codes	Xi
HS Code	2926909090

79-08-3

873-74-5

~88%

42288-26-6

Literature: ZENTIVA, K.S. Patent: WO2009/111997 A1, 2009 ; Location in patent: Page/Page column 11 ;

79-11-8

873-74-5

~56%

42288-26-6

Literature: Dolle, Roland E.; Chu, Guo-Hua; Gu, Minghua Patent: US2005/107355 A1, 2005 ; Location in patent: Page/Page column 30 ;

3926-62-3

873-74-5

~72%

42288-26-6

Literature: MEDICHEM S.A.; SERRA MIRALLES, Judit; DURAN LOPEZ, Ernesto; RAO, Lingxiang Patent: WO2012/152855 A1, 2012 ; Location in patent: Page/Page column 34; 36-37 ;

144656-11-1

42288-26-6

Literature: Sall, Daniel J.; Arfsten, Ann E.; Bastian, Jolie A.; Denney, Michael L.; Harms, Cathy S.; McCowan, Jefferson R.; Morin Jr., John M.; Rose, Jack W.; Scarborough, Robert M.; Smyth, Mark S.; Um, Suzane L.; Utterback, Barbara G.; Vasileff, Robert T.; Wikel, James H.; Wyss, Virginia L.; Jakubowski, Joseph A. Journal of Medicinal Chemistry, 1997 , vol. 40, # 18 p. 2843 - 2857

873-74-5

42288-26-6

Literature: Sall, Daniel J.; Arfsten, Ann E.; Berry, Dennis R.; Denney, Michael L.; Harms, Cathy S.; McCowan, Jefferson R.; Ray, Judith K.; Scarborough, Robert M.; Um, Suzane L.; Utterback, Barbara G.; Jakubowski, Joseph A. Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 1 p. 81 - 86

Precursor 5
79-08-3 873-74-5 79-11-8 3926-62-3
144656-11-1
DownStream 4
872728-81-9 211915-06-9 211915-84-3 851680-14-3

HS Code	2926909090
Summary	HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

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