Boc-L-aspartic acid 4-benzyl ester

Modify Date: 2024-01-02 21:20:00

Boc-L-aspartic acid 4-benzyl ester Structure
Boc-L-aspartic acid 4-benzyl ester structure
 Common Name Boc-L-aspartic acid 4-benzyl ester
CAS Number 7536-58-5 Molecular Weight 323.341
Density 1.2±0.1 g/cm3 Boiling Point 508.1±50.0 °C at 760 mmHg
Molecular Formula C16H21NO6 Melting Point 98-102ºC
MSDS USA Flash Point 261.1±30.1 °C

 Use of Boc-L-aspartic acid 4-benzyl ester


(2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1].

 Names

Name Boc-L-Asp(OBzl)-OH
Synonym More Synonyms

 Boc-L-aspartic acid 4-benzyl ester Biological Activity

Description (2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1].
Related Catalog
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 508.1±50.0 °C at 760 mmHg
Melting Point 98-102ºC
Molecular Formula C16H21NO6
Molecular Weight 323.341
Flash Point 261.1±30.1 °C
Exact Mass 323.136902
PSA 101.93000
LogP 3.24
Vapour Pressure 0.0±1.4 mmHg at 25°C
Index of Refraction 1.527

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090

 Synthetic Route

 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%

 Articles3

More Articles
Vitamin K1 dependent carboxylase: beta-carboxylation of t-butyloxycarbonylaspartic acid alpha-benzyl ester.

Biochem. Biophys. Res. Commun. 107(1) , 246-9, (1982)

Vitamin K-dependent carboxylase. Carboxylation of aspartyl residues to beta-carboxyaspartyl residues in synthetic substrates.

J. Biol. Chem. 259(7) , 4272-8, (1984)

The rat liver microsomal vitamin K-dependent carboxylase has been shown to carboxylate the aspartyl residue in N alpha-t-butyloxycarbonylaspartic acid alpha-benzyl ester to a beta-carboxyaspartyl resi...

Transesterification and amide cis-trans isomerization in Zn and Cd complexes of the chelating amino acid ligand Boc-Asp(Dpa)-OBzl.

Dalton Trans. (1) , 154-62, (2007)

The amino acid derivative Boc-Asp-OBzl (Boc=N-butyloxycarbonyl; Asp=aspartic acid; Bzl=benzyl) was functionalized by coupling its carboxylate side chain to dipicolylamine. This yielded the tridentate ...

 Synonyms

(2S)-4-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
EINECS 231-406-8
N-tert-Butoxycarbonyl-L-aspartic acid 4-benzyl ester
MFCD00065564
(2S)-4-(Benzyloxy)-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid
L-Aspartic acid, N-((1,1-dimethylethoxy)carbonyl)-, 4-(phenylmethyl) ester
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(phenylmethyl) ester
N-α-t-BOC-L-aspartic-β-benzyl ester
Boc-Asp(OBzl)-OH
Boc-L-asparticacid4-benzylester
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