CAS 7536-58-5|Boc-L-aspartic acid 4-benzyl ester

Introduction:Basic information about CAS 7536-58-5|Boc-L-aspartic acid 4-benzyl ester, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBoc-L-aspartic acid 4-benzyl ester
CAS Number7536-58-5Molecular Weight323.341
Density1.2±0.1 g/cm3Boiling Point508.1±50.0 °C at 760 mmHg
Molecular FormulaC16H21NO6Melting Point98-102ºC
MSDSUSAFlash Point261.1±30.1 °C

Names

NameBoc-L-Asp(OBzl)-OH
SynonymMore Synonyms

Boc-L-aspartic acid 4-benzyl ester BiologicalActivity

Description(2S)-4-(Benzyloxy)-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid is an aspartic acid derivative[1].
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others
In VitroAmino 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

Density1.2±0.1 g/cm3
Boiling Point508.1±50.0 °C at 760 mmHg
Melting Point98-102ºC
Molecular FormulaC16H21NO6
Molecular Weight323.341
Flash Point261.1±30.1 °C
Exact Mass323.136902
PSA101.93000
LogP3.24
Vapour Pressure0.0±1.4 mmHg at 25°C
Index of Refraction1.527
InChIKeySOHLZANWVLCPHK-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)NC(CC(=O)OCc1ccccc1)C(=O)O

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXn
Safety PhrasesS22-S24/25
RIDADRNONH for all modes of transport
WGK Germany3
HS Code2924299090

Customs

HS Code2924299090
Summary2924299090. 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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