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Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid is a specialized chemical compound integral to the field of peptide synthesis and research. Characterized by the presence of a fluorinated aromatic ring and a butyric acid side chain with an amino group, Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid is distinguished by its unique chemical properties. The Fmoc group, a protecting group widely utilized in peptide chemistry, shields the amine group from undesired reactions, thereby facilitating controlled peptide synthesis. Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid holds significant value for the development of peptide-based drugs and materials, as well as for the study of protein structure and function, making it a key component in the pharmaceutical and biotechnology industries.

269726-72-9

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269726-72-9 Usage

Uses

Used in Pharmaceutical Industry:
Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid serves as a crucial building block in the synthesis of peptide-based drugs. Its incorporation into peptide sequences allows for the creation of novel therapeutic agents with specific biological activities, tailored to target various diseases and conditions.
Used in Biotechnology Industry:
In the biotechnology sector, Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid is utilized for the development of advanced materials and for studying the structure-function relationships of proteins. Its unique properties enable researchers to probe and understand the intricate mechanisms of protein interactions and functions, thereby contributing to the advancement of biotechnological applications.
Used in Peptide Synthesis Research:
Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid is employed as a research tool in the field of peptide synthesis. It aids scientists in exploring new methods and techniques for the assembly of peptides, with the aim of improving the efficiency, specificity, and yield of peptide synthesis processes.
Used in Drug Development:
Fmoc-(R)-3-Amino-4-(2-trifluoromethyl-phenyl)-butyric acid is used as a key component in the design and synthesis of new drugs, particularly those that require the specific properties conferred by the presence of a fluorinated aromatic ring. Its unique structure allows for the modulation of drug-target interactions, potentially leading to the development of more effective and selective therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 269726-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,7,2 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 269726-72:
(8*2)+(7*6)+(6*9)+(5*7)+(4*2)+(3*6)+(2*7)+(1*2)=189
189 % 10 = 9
So 269726-72-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H22F3NO4/c27-26(28,29)23-12-6-1-7-16(23)13-17(14-24(31)32)30-25(33)34-15-22-20-10-4-2-8-18(20)19-9-3-5-11-21(19)22/h1-12,17,22H,13-15H2,(H,30,33)(H,31,32)/t17-/m1/s1

269726-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-(R)-3-amino-4-(2-trifluoromethylphenyl)-butyric acid

1.2 Other means of identification

Product number -
Other names Fmoc-D-b-HoPhe(2-CF3)-OH

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:269726-72-9 SDS

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