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35661-40-6

35661-40-6 structure
35661-40-6 structure

Name FMOC-L-Phenylalanine
Synonyms Fmoc-L-Phc-OH
N-FMOC-PHE-OH
EINECS 252-661-1
L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-Fmoc-(S)-phenylalanine
FMOC-L-PHE-OH
FMOC-L-PHE
N-Fmoc-L-Phe-OH
MFCD00037128
9-fluorenylmethyloxycarbonyl-Phe-OH
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylpropanoic acid
N-FMOC-L-PHE
N-Fmoc-L-phenylalanine
FMOC-PHENYLALANINE
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
Fmoc-Phe-OH
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-3-phenyl-L-alanine
N-9-Fmoc-L-phenylglycine
FMOC-PHE
N-Fmoc-Phe-OH ( N-Fmoc-L-phenylalanine)
Description Fmoc-Phe-OH is a phenylalanine 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):1793-816.

Density 1.3±0.1 g/cm3
Boiling Point 620.1±50.0 °C at 760 mmHg
Melting Point 180-187 °C(lit.)
Molecular Formula C24H21NO4
Molecular Weight 387.428
Flash Point 328.8±30.1 °C
Exact Mass 387.147064
PSA 75.63000
LogP 5.41
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.633
Storage condition 2~8°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2924299090
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%