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135944-09-1

135944-09-1 structure
135944-09-1 structure

Name Fmoc-D-homophenylalanine
Synonyms FMOC-D-HOPHE-OH
(2S)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-phenylbutanoic acid
FMOC-D-HPH-OH
F-moc-D-homophenylalanine-OH
FMOC-D-HPHE-OH
Benzenebutanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-
FMOC-D-HPHE
Fmoc-D-homo-phenylalanine
RARECHEM BK PT 0054
N-FMOC-D-HOMOPHE-OH
MFCD00151917
Fmoc-D-Homophe-OH
FMOC-D-HFE-OH
Fmoc-S-homophenylalanine
(2R)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-4-phenylbutanoic acid
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-phenylbutanoic acid
Benzenebutanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-
Fmoc-D-HoPhe-PH
Fmoc-S-hPhe-OH
FMOC-D-HOMOPHE
Description Fmoc-D-HoPhe-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):1793-850.

Density 1.3±0.1 g/cm3
Boiling Point 628.3±50.0 °C at 760 mmHg
Molecular Formula C25H23NO4
Molecular Weight 401.454
Flash Point 333.8±30.1 °C
Exact Mass 401.162720
PSA 75.63000
LogP 5.89
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.624
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
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%