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205526-38-1

205526-38-1 structure
205526-38-1 structure

Name fmoc-l-4,4'-biphenylalanine
Synonyms (2R)-3-(4-Biphenylyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
FMOC-D-BPH-OH
FMOC-L-BIP-OH
FMOC-BIP-OH
FMOC-D-BIP(4,4')-OH
FMOC-4-PHENYL-PHE-OH
(2S)-3-(Biphenyl-4-yl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid (non-preferred name)
FMOC-L-PHE(4-PH)-OH
Fmoc-D-phe(4-ph)-OH
3-(4-Biphenylyl)-N-Fmoc-D-alanine
FMOC-BIP(4,4')-OH
FMOC-BPH-OH
(2R)-3-(Biphenyl-4-yl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid (non-preferred name)
FMOC-L-PHE(4-PH)
(2S)-3-(4-Biphenylyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-4,4'-biphenylalanine
MFCD00191198
FMOC-D-BIP-OH
Fmoc-D-Bip(4,4)-OH
Description Fmoc-D-Bip(4,4’)-OH is an alanine 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):1793-1074.

Density 1.3±0.1 g/cm3
Boiling Point 700.7±60.0 °C at 760 mmHg
Molecular Formula C30H25NO4
Molecular Weight 463.524
Flash Point 377.6±32.9 °C
Exact Mass 463.178345
PSA 75.63000
LogP 7.16
Vapour Pressure 0.0±2.3 mmHg at 25°C
Index of Refraction 1.641
Storage condition 2-8°C
Hazard Codes Xi