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84000-14-6

84000-14-6 structure
84000-14-6 structure

Name N-Fmoc-N-methyl-O-benzyl-L-serine
Synonyms N-(9-Fluorenylmethyloxycarbonyl)-N-methyl-O-benzyl-L-serine
FMOC-O-BENZYL-N-METHYL-L-SERINE
Fmoc-Meser(Bzl)-OH
FMOC-N-ME-SER(BZL)-OH
O-Benzyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-serine
FMOC-N-METHYL-O-BENZYL-L-SERINE
FMOC-L-MESER(BZL)-OH
FMOC-N-ME-SER(BZL)
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-O-(phenylmethyl)-L-serine
Fmoc-N(Me)-Ser(Bn)
L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-O-(phenylmethyl)-
Fmoc-N-Me-Ser(OBz)-OH
Description Fmoc-MeSer(Bzl)-OH 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.

Density 1.3±0.1 g/cm3
Boiling Point 618.9±55.0 °C at 760 mmHg
Molecular Formula C26H25NO5
Molecular Weight 431.480
Flash Point 328.1±31.5 °C
Exact Mass 431.173279
PSA 76.07000
LogP 6.49
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.618
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
Precursor  2

DownStream  0