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1913-12-8

1913-12-8 structure
1913-12-8 structure

Name Boc-Asp(OtBu)-OH DCHA
Synonyms BOC-L-ASPARTIC ACID-B-T-BUTYLESTER DCHA SALT
BOC-L-ASP(TBU)-OH DCHA
4-tert-butyl hydrogen N-[(tert-butoxy)carbonyl]-L-aspartate
4-tert-Butyl N-[(tert-butoxy)carbonyl]-L-aspartate dicyclohexylamine salt
Boc-L-Asp(OtBu)-OH (dicyclohexylammonium) salt
Einecs 217-626-7
(2S)-4-tert-Butoxy-2-[(tert-butoxycarbonyl)amino]-4-oxobutanoic acid - N-cyclohexylcyclohexanamine (1:1) (non-preferred name)
Boc-Asp(O-t-Bu)-OH dicyclohexylamine salt
N-T-BOC-L-ASPARTICACIDB-T-BUTYLESTEROICYCLOHE
MFCD00038889
Boc-L-Asp(OtBu)-OH dicyclohexylamine salt
compound with dicyclohexylamine (1:1)
BOC-ASP(OTBU)-OHCHA
BOC-L-ASP(OTBU)-OH DCHA
Boc-Asp(OtBu)-OH.DCHA
BOC-ASP(OBUT)-OH DCHA
Boc-Asp(OtBu)-OH·DCHA
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(1,1-dimethylethyl) ester, compd. with N-cyclohexylcyclohexanamine (1:1)
(2S)-4-[(2-Methyl-2-propanyl)oxy]-2-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-4-oxobutanoic acid - N-cyclohexylcyclohexanamine (1:1)
Boc-Asp(OtBu)-OH• tert-butyl-N-tert-butyloxycarbonyl-L-aspartate dicyclohexylammonium salt
4-tert-ButylN-[(tert-butoxy)carbonyl]-L-aspartatedicyclohexylaminesalt
Description Boc-Asp(OtBu)-OH.DCHA 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.

Molecular Formula C25H46N2O6
Molecular Weight 470.642
Exact Mass 470.335602
PSA 113.96000
LogP 5.71930
Vapour Pressure 2.47E-16mmHg at 25°C
Storage condition −20°C
Hazard Codes T+
WGK Germany 3
Precursor  0

DownStream  2