N-tert-Butoxycarbonyl-L-aspartic acid 1-methyl ester

Names

[ Name ]:
N-tert-Butoxycarbonyl-L-aspartic acid 1-methyl ester

[Synonym ]:
N-tert-Butoxycarbonyl-L-aspartic acid 1-methyl ester
2-Bromo-4-methylbenzoic acid
4-methyl-2-bromobenzoic acid
Boc-Asp-OMe
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-methyl ester
2-Brom-p-toluylsaeure
N-BOC ASP(OH)OME
BOC-ASP.OME
2-Brom-4-methyl-benzoesaeure
Benzoic acid, 2-bromo-4-methyl-
N-tert-Butoxycarbonyla spartic acid a-methylester
2-bromo-4-methyl-benzoic acid
bromo-p-toluic acid
(3S)-4-Methoxy-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
2-Bromo-p-toluic Acid
N-Boc-L-aspartic acid 1-Methyl ester

Biological Activity

[Description]:

Boc-Asp-OMe 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]:
1.2±0.1 g/cm3

[ Boiling Point ]:
407.1±40.0 °C at 760 mmHg

[ Melting Point ]:
79-81°C

[ Molecular Formula ]:
C₁₀H₁₇NO₆

[ Molecular Weight ]:
247.245

[ Flash Point ]:
200.0±27.3 °C

[ Exact Mass ]:
247.105591

[ PSA ]:
101.93000

[ LogP ]:
1.49

[ Vapour Pressure ]:
0.0±2.0 mmHg at 25°C

[ Index of Refraction ]:
1.470

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi