331763-76-9 Usage
General Description
FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is a chemical compound consisting of a fluorenylmethyloxycarbonyl (FMOC) protecting group, an amino group, and a butyric acid moiety with a bromophenyl substituent. The FMOC group is commonly used to protect amine functionalities in peptide synthesis, while the butyric acid moiety provides a carboxylic acid functionality. The presence of the 4-bromo-phenyl group makes this compound potentially useful in the development of bioconjugates or peptide-based drugs. The (R) configuration indicates that the chiral center in the molecule is in the R stereochemistry, which may be important for biological activity or specificity. Overall, FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is a versatile chemical that could have applications in peptide synthesis, medicinal chemistry, or bioconjugation.
Check Digit Verification of cas no
The CAS Registry Mumber 331763-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,1,7,6 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 331763-76:
(8*3)+(7*3)+(6*1)+(5*7)+(4*6)+(3*3)+(2*7)+(1*6)=139
139 % 10 = 9
So 331763-76-9 is a valid CAS Registry Number.
331763-76-9Relevant articles and documents
Synthesis of β3-homophenylalanine-derived amino acids and peptides by Suzuki coupling in solution and on solid support
Limbach, Michael,Loeweneck, Markus,Schreiber, Juerg V.,Frackenpohl, Jens,Seebach, Dieter,Billich, Andreas
, p. 1427 - 1441 (2007/10/03)
β-Peptides and, to a certain extent, also mixed α,β- peptides, are resistant to degradation by a variety of proteolytic enzymes that rapidly degrade natural α-peptides. This is one of many characteristics that make β-peptides an attractive class of compou
