CAS 32991-17-6|N-[(1,1-Dimethylethoxy)carbonyl]-L-leucylglycine

Introduction:Basic information about CAS 32991-17-6|N-[(1,1-Dimethylethoxy)carbonyl]-L-leucylglycine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameN-[(1,1-Dimethylethoxy)carbonyl]-L-leucylglycine
CAS Number32991-17-6Molecular Weight288.340
Density1.1±0.1 g/cm3Boiling Point499.6±30.0 °C at 760 mmHg
Molecular FormulaC13H24N2O5Melting Point/
MSDS/Flash Point255.9±24.6 °C

Names

Name2-[[(2S)-4-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoyl]amino]acetic acid
SynonymMore Synonyms

BiologicalActivity

Description(tert-Butoxycarbonyl)-L-leucylglycine is a Glycine (HY-Y0966) 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

Density1.1±0.1 g/cm3
Boiling Point499.6±30.0 °C at 760 mmHg
Molecular FormulaC13H24N2O5
Molecular Weight288.340
Flash Point255.9±24.6 °C
Exact Mass288.168518
PSA104.73000
LogP1.69
Vapour Pressure0.0±2.7 mmHg at 25°C
Index of Refraction1.478
InChIKeyNRXDUMDULDHIEA-VIFPVBQESA-N
SMILESCC(C)CC(NC(=O)OC(C)(C)C)C(=O)NCC(=O)O
Storage condition2-8°C

Safety Information

Hazard CodesXi
HS Code2924199090

Customs

HS Code2924199090
Summary2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Synonyms

BOC-LEU-GLY-OH
N-Boc-Leu-Gly-OH
Glycine, N-[(1,1-dimethylethoxy)carbonyl]-L-leucyl-
Boc-L-leucyl-glycine
Boc-Leu-Gly-COOH
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-leucylglycine
Boc-Leu-Gly
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