CAS 92828-64-3|Boc-D-Asp-OBzl

Introduction:Basic information about CAS 92828-64-3|Boc-D-Asp-OBzl, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameBoc-D-Asp-OBzl
CAS Number92828-64-3Molecular Weight323.341
Density1.2±0.1 g/cm3Boiling Point504.3±50.0 °C at 760 mmHg
Molecular FormulaC16H21NO6Melting Point/
MSDSChineseFlash Point258.8±30.1 °C

Names

Name(3R)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxo-4-phenylmethoxybutanoic acid
SynonymMore Synonyms

Boc-D-Asp-OBzl BiologicalActivity

DescriptionBoc-D-Asp-OBzl 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 Point504.3±50.0 °C at 760 mmHg
Molecular FormulaC16H21NO6
Molecular Weight323.341
Flash Point258.8±30.1 °C
Exact Mass323.136902
PSA101.93000
LogP3.34
Vapour Pressure0.0±1.4 mmHg at 25°C
Index of Refraction1.527
InChIKeyLDRWTKQWSXGSTM-GFCCVEGCSA-N
SMILESCC(C)(C)OC(=O)NC(CC(=O)O)C(=O)OCc1ccccc1
Storage conditionStore at RT.

Safety Information

Hazard CodesT+
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%

Synonyms

(3S)-4-(Benzyloxy)-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
Boc-D-Asp-OBzl ester
BOC-D-ASP(OBZL)-OH
MFCD00038255
(3R)-4-(Benzyloxy)-3-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester
Boc-(D)-Asp-OBn
Boc-D-aspartic acid 1-benzyl ester
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester
Boc-D-Asp-OBzl
Boc-D-aspartic acid a-benzyl ester
(3S)-4-(Benzyloxy)-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
(3R)-4-(benzyloxy)-3-{[(tert-butoxy)carbonyl]amino}-4-oxobutanoic acid
(R)-2-tert-butoxycarbonylamino-succinic acid 1-benzyl ester
Boc-L-Asp-OBzl
(3R)-4-(Benzyloxy)-3-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
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