<Suppliers Price>

Fmoc-Leu-OPfp

Names

[ CAS No. ]:
86060-88-0

[ Name ]:
Fmoc-Leu-OPfp

[Synonym ]:
Fmoc-Leu-OPf
Fmoc-L-leucine pentafluorophenyl ester
pentafluorophenyl L-N-[(9H-fluoren-9-ylmethoxy)carbonyl]leucinate
fluorenylmethoxycarbonyl-L-leucine pentafluorophenyl ester
Fmoc-Leu-OPfp
N-(9-fluorenylmethoxycarbonyl)-L-leucine pentafluorophenyl ester
MFCD00065658

Biological Activity

[Description]:

Fmoc-Leu-OPfp is a leucine derivative[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[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.

Chemical & Physical Properties

[ Density]:
1.35 g/cm3

[ Boiling Point ]:
596.3ºC at 760 mmHg

[ Molecular Formula ]:
C27H22F5NO4

[ Molecular Weight ]:
519.46000

[ Flash Point ]:
314.5ºC

[ Exact Mass ]:
519.14700

[ PSA ]:
64.63000

[ LogP ]:
6.63180

[ Index of Refraction ]:
1.549

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Related Compounds