FMOC-D-PHE(4-TBU)-(C*CH2)OH

FMOC-D-PHE(4-TBU)-(C*CH2)OH - Names and Identifiers

Name	Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid
Synonyms	RARECHEM AK PT F134 Fmoc-D-b-HoPhe(4-tBu)-OH FMOC-D-BETA-HOPHE(4-TBU)-OH FMOC-D-PHE(4-TBU)-(C*CH2)OH FMOC-(R)-3-AMINO-4-(4-TERT-BUTYL-PHENYL)-BUTYRIC ACID FMOC-(R)-3-AMINO-4-(4-TERT-BUTYL-PHENYL)BUTANOIC ACID Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid (9H-Fluoren-9-yl)MethOxy]Carbonyl (R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid (R)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-3-AMINO-4-(4-TERT-BUTYL-PHENYL)-BUTYRIC ACID
CAS	401916-49-2

FMOC-D-PHE(4-TBU)-(C*CH2)OH - Physico-chemical Properties

Molecular Formula	C29H31NO4
Molar Mass	457.56

FMOC-D-PHE(4-TBU)-(C*CH2)OH - Introduction

Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid is an organic compound with the chemical formula C26H27NO3.

In terms of nature, it is a white solid with fat solubility. It is an amino acid containing a protecting group, wherein Fmoc is an amino protecting group.

Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid is mainly used for peptide synthesis in biochemical and medicinal chemistry research. It can be used as a prodrug for the preparation of biologically active polypeptides and proteins.

Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid can be synthesized by various synthetic methods. A common method is to react R-3-amino -4 (4-tert-butylphenyl)-butyric acid with Fmoc-phosgenic methanamic anhydride using appropriate reagents and reaction conditions to form the target compound.

For safety information, Fmoc-(R)-3-Amino-4-(4-tert-butyl-phenyl)-butyric acid is not currently classified as a particularly hazardous or toxic substance. However, when using or handling chemicals, appropriate laboratory safety procedures should still be followed, and care should be taken to prevent inhalation, ingestion or contact with skin and eyes. In case of discomfort, seek medical help immediately.

Last Update：2024-04-10 22:30:50