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FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is a versatile chemical compound that features a fluorenylmethyloxycarbonyl (FMOC) protecting group, an amino group, and a butyric acid moiety with a 4-bromo-phenyl substituent. The FMOC group is utilized to protect amine functionalities during peptide synthesis, while the butyric acid component offers a carboxylic acid functionality. The 4-bromo-phenyl group enhances the compound's potential for use in the creation of bioconjugates or peptide-based drugs. The (R) configuration of the chiral center is significant for the compound's biological activity and specificity. This chemical is well-suited for applications in peptide synthesis, medicinal chemistry, and bioconjugation.

331763-76-9

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331763-76-9 Usage

Uses

Used in Peptide Synthesis:
FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is used as a protected amino acid for peptide synthesis, where the FMOC group shields the amine group from unwanted reactions until it is deprotected at the appropriate stage of the synthesis process.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is used as a building block for the design and synthesis of novel peptide-based drugs, leveraging its unique structural features to target specific biological receptors or enzymes.
Used in Bioconjugation:
FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is utilized as a linker or a component in the development of bioconjugates, which are hybrid molecules combining biologically active compounds with other molecules, such as fluorescent tags or therapeutic agents, for various applications in research and medicine.
Used in Pharmaceutical Development:
In the pharmaceutical industry, FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID is used as a key intermediate in the synthesis of new drug candidates, taking advantage of its chemical properties to create molecules with improved pharmacological profiles, including enhanced potency, selectivity, and pharmacokinetics.

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.

331763-76-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-3-amino-4-(4-bromophenyl)-2-(9H-fluoren-9-ylmethoxycarbonyl)butanoic acid

1.2 Other means of identification

Product number -
Other names FMOC-(R)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRICACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:331763-76-9 SDS

331763-76-9Downstream Products

331763-76-9Relevant academic research and scientific papers

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

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