H-Asp(OMe)-OH·HCl

Names

[ Name ]:
H-Asp(OMe)-OH·HCl

[Synonym ]:
(2S)-2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride (1:1)
L-Aspartatic Acid 4-Methyl Ester Hydrochloride
4-Methyl L-Aspartate Hydrochloride
EINECS 240-880-5
L-Asparitc acid 4-methyl ester HCl
L-Aspartic acid, 4-methyl ester, hydrochloride (1:1)
MFCD00038972
H-Asp(OMe)-OH.HCl
H-Asp(OMe)-OH·HCl
(S)-2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride
beta-Methyl L-aspartate hydrochloride
β-Methyl L-aspartate hydrochloride

Biological Activity

[Description]:

β-Methyl L-aspartate hydrochloride is an aspartic acid 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]:
1.299g/cm3

[ Boiling Point ]:
301.7ºC at 760mmHg

[ Melting Point ]:
191-193°C

[ Molecular Formula ]:
C₅H₁₀ClNO₄

[ Molecular Weight ]:
183.590

[ Flash Point ]:
136.3ºC

[ Exact Mass ]:
183.029831

[ PSA ]:
89.62000

[ LogP ]:
0.46370

[ Vapour Pressure ]:
0.000242mmHg at 25°C

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922509090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Syntheses of S-enantiomers of hanishin, longamide B, and longamide B methyl ester from L-aspartic acid beta-methyl ester: establishment of absolute stereochemistry.

J. Org. Chem. 70 , 9081-9084, (2005)

[reaction: see text] Total syntheses of enantiopure hanishin, longamide B, and longamide B methyl ester are described. Absolute configurations of these natural products have been established.

Enzymatic synthesis of a CCK-4 tripeptide fragment.

Di Yi Jun Yi Da Xue Xue Bao 23 , 289-292, (2003)

To synthesize a tripeptide derivative Phac-Met-Asp(OMe)-Phe -NH2, which is a fragment of the gastrin C-terminal tetrapeptide CCK-4, by enzymatic reaction.Three free enzymes, alpha-chymotrypsin, papain...

Practical synthesis of (R)-4-mercaptopyrrolidine-2-thione from L-aspartic acid. Preparation of a novel orally active 1-beta-methylcarbapenem, TA-949.

J. Org. Chem. 65 , 517-522, (2000)

A facile and economical synthesis of a novel orally active 1-beta-methylcarbapenem, TA-949 (1), is described. The key process involves an efficient synthesis of the C-2 side chain (R)-4-mercaptopyrrol...

Related Compounds

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