95753-55-2

95753-55-2 structure

Name: N-Fmoc-4-Nitro-L-Phenylalanine
Chemical Name: N-Fmoc-4-Nitro-L-Phenylalanine
CAS Number: 95753-55-2
Molecular Formula: C₂₄H₂₀N₂O₆
Molecular Weight: 432.425
Catalog: Biochemical Amino acids and their derivatives Phenylalanine derivatives
Create Date: 2018-03-28 08:00:00
Modify Date: 2024-01-08 17:40:14
Fmoc-Phe(4-NO2)-OH is a phenylalanine derivative[1].

Name	N-Fmoc-4-Nitro-L-Phenylalanine
Synonyms	(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-nitrophenyl)propanoic acid MFCD00057810 Fmoc-D-phe(4-NO2)-OH L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-nitro- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine Fmoc-Phe(4-NO2)-OH Fmoc-4-nitro-L-phenylalanine Fmoc-Phe(4-NO2)-OH H2O

Description	Fmoc-Phe(4-NO2)-OH is a phenylalanine 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):1793-908.

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	Xi: Irritant;
Safety Phrases	S22-S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3

28920-43-6

949-99-5

~84%

95753-55-2

Literature: Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), , # 10 p. 1723 - 1728

949-99-5

82911-69-1

~84%

95753-55-2

Literature: Tetrahedron Letters, , vol. 40, # 36 p. 6557 - 6560