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111061-55-3

111061-55-3 structure
111061-55-3 structure

Name Fmoc-Hse(Trt)-OH
Synonyms N-Fmoc-L-HSE(OTrt)-OH
Fmoc-N-methyl-D-valine
Fmoc(OTrt)homoserine
Fmoc-Homoser(Trt)-OH
Fmoc-O-trityl-L-homoserine
Fmoc-(N-Me)Val-OH
Fmoc-HoSer(Trt)-OH
fmoc-N-methyl-L-valine
Fmoc-Hse(Tr)-OH
Fmoc-(S)-NMeVal-OH
Fmoc-N-Me-L-Val-OH
MFCD00270544
Fmoc-N-methylvaline
N-Fmoc-OTrt-L-homoserine
Fmoc-D-N-Me-Val-OH
N-Fmoc-N-methyl-L-valine
TMA023
N-Fmoc-O-trityl-L-homoserine
Fmoc-N-Me-D-Val-OH
Fmoc-L-N-MeVal-OH
Description N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-trityl-L-homoserine 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 1.242g/cm3
Boiling Point 767.5ºC at 760 mmHg
Melting Point 63-66 °C
Molecular Formula C38H33NO5
Molecular Weight 583.67200
Flash Point 418ºC
Exact Mass 583.23600
PSA 84.86000
LogP 7.76800
Vapour Pressure 8.97E-25mmHg at 25°C
Index of Refraction 1.632
Storage condition 2-8°C
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 2924299090
Precursor  2

DownStream  0

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%