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1676-90-0

1676-90-0 structure
1676-90-0 structure

Name Boc-Asp(OtBu)-OH
Synonyms Boc-Asp(Otbu)-OH
N-(tert-Butoxycarbonyl)-L-aspartic Acid 4-tert-Butyl Ester
4-tert-Butyl N-Boc-L-aspartate
N-Boc-L-aspartic Acid 4-tert-Butyl Ester
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester
4-tert-Butyl N-(tert-Butoxycarbonyl)-L-aspartate
N-Alpha-t-Boc-L-aspartic acid beta-t-butyl ester
(2S)-4-tert-Butoxy-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid (non-preferred name)
(2S)-4-[(2-Methyl-2-propanyl)oxy]-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid
N-Alpha-t-Boc-L-aspartic
Boc-L-aspartic acid 4-tert-butyl ester
MFCD00076912
Boc-L-aspartic acid 4-tert-butylester
Description Boc-Asp(OtBu)-OH 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.

Density 1.1±0.1 g/cm3
Boiling Point 432.6±40.0 °C at 760 mmHg
Melting Point 64-67 °C
Molecular Formula C13H23NO6
Molecular Weight 289.325
Flash Point 215.4±27.3 °C
Exact Mass 289.152527
PSA 101.93000
LogP 2.72
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.470
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924199090
HS Code 2924199090
Summary 2924199090. 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%