109434-27-7

109434-27-7 structure
109434-27-7 structure

Name Fmoc-O-tert-Butyl-L-serine 3,4-dihydro-4-oxo-1,2,3-benzotriazin-3-yl ester
Synonyms FMOC-butyl-L-serine 3,4-dihydro-4-oxo-1,2,3-benzotriazine
N-FMOC-O-T-BUTYL-L-SERINE 3,4-*DIHYDRO-4-OXO-1,2,3
Fmoc-Ser(But)-ODhbt
Fmoc-O-tert-butyl-L-serine 3,4-dihydro-4-oxo-1,2,3-benzotriazin-3-ylester
FMOC-SER(TBU)-ODHBT
FMOC-O-T-BUTYL-L-SERINE 3,4-DIHYDRO-3-HYDROXY-4-OXO-1,2,3-BENZOTRIAZINE ESTER
N-fmoc-O-T-butyl-L-serine 3,4-*dihydro-4-oxo-1,2
FMOC-SERINE(TBU)-ODHBT
N-FMOC-O-T-BUTYL-L-SERINE 3,4-DIHYDRO-4-OXO-1,2,3-BENZOTRIAZINE ESTER
MFCD00133600
Fmoc-O-tert-butyl-L-serine3,4-Dihydro-4-oxo-1,2,3
Fmoc-Ser(tBu)-OObt
Description Fmoc-Ser(tBu)-ODhbt is a serine 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.

Melting Point 67-70ºC (dec.)
Molecular Formula C29H28N4O6
Molecular Weight 528.55600
Exact Mass 528.20100
PSA 121.64000
LogP 3.86000
Storage condition 2-8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3