(2R)-Amino(3,5-dinitrophenyl)acetic acid

Names

[ Name ]:
(2R)-Amino(3,5-dinitrophenyl)acetic acid

[Synonym ]:
(2R)-2-[(3,5-dinitrobenzoyl)amino]-2-phenylacetic acid
(2R)-Amino(3,5-dinitrophenyl)acetic acid
Benzeneacetic acid, α-amino-3,5-dinitro-, (αR)-
MFCD00010134

Biological Activity

[Description]:

(2R)-2-[(3,5-Dinitrobenzoyl)amino]-2-phenyl-acetic acid 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.

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
421.4±45.0 °C at 760 mmHg

[ Melting Point ]:
217-218 °C (dec.)

[ Molecular Formula ]:
C₁₅H₁₁N₃O₇

[ Molecular Weight ]:
241.158

[ Flash Point ]:
208.6±28.7 °C

[ Exact Mass ]:
241.033478

[ PSA ]:
158.04000

[ LogP ]:
0.34

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.667

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2924299090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2924299090

[ Summary ]:
2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

A screening method for chiral selectors that does not require covalent attachment.

J. Am. Chem. Soc. 128(7) , 2208-9, (2006)

A high-throughput screening protocol is proposed for chiral selector discovery. It is modeled after the protocol for biological screening of candidate drugs from chemical libraries. The procedure work...

Resolution of enantiomers of 19-hydroxyeicosatetraenoate and 18-hydroxyeicosatetraenoate by chiral phase high-performance liquid chromatography of naphthoyl ester derivatives.

J. Chromatogr. A. 526(2) , 525-9, (1990)

QSAR of matrix metalloproteinase inhibitor N-[(substituted phenyl)sulfonyl]-N-4-nitrobenzylglycine hydroxamates using LFER model.

Drug Des. Discov. 17(4) , 315-23, (2001)

QSAR analyses of matrix metalloproteinase (MMP) inhibitor N-[(substituted phenyl)sulfonyl]-N-4-nitrobenzylglycine hydroxamates, recently reported by Scozzafava and Supuran, have been attempted using l...