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Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is a specialized chemical compound in the realm of organic chemistry, characterized by its unique structure that includes a butyric acid backbone, an amino group, a benzothienyl moiety, and the Fmoc protecting group. Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is distinguished by its stereochemistry and serves as a versatile building block in the synthesis of peptides and other complex organic molecules.

270063-46-2

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270063-46-2 Usage

Uses

Used in Pharmaceutical Development:
Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is used as a key component in the solid-phase synthesis of peptides for its ability to facilitate the controlled formation of peptide bonds. Its unique structural features and stereochemistry contribute to the creation of diverse peptide sequences with specific functionalities, making it an essential tool in the development of new pharmaceuticals and bioactive compounds.
Used in Organic Chemistry Research:
In the field of organic chemistry, Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is utilized as a building block for the synthesis of complex organic molecules. Its presence allows for the exploration of novel chemical reactions and the synthesis of new compounds with potential applications in various industries.
Used in Peptide Synthesis:
Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is used as a crucial building block in peptide synthesis, particularly in solid-phase peptide synthesis techniques. Its role is pivotal for the controlled and stepwise assembly of peptide chains, which is vital for the production of peptides with well-defined sequences and structures.
Used in Biochemistry and Molecular Biology:
Fmoc-(S)-3-Amino-4-(3-benzothienyl)-butyric acid is also used in biochemical and molecular biology research to study the interactions of peptides with various biomolecules, such as proteins and nucleic acids. Its unique structural features allow for the investigation of molecular recognition and binding processes, contributing to a deeper understanding of biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 270063-46-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,0,6 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 270063-46:
(8*2)+(7*7)+(6*0)+(5*0)+(4*6)+(3*3)+(2*4)+(1*6)=112
112 % 10 = 2
So 270063-46-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H23NO4S/c29-26(30)14-18(13-17-16-33-25-12-6-5-7-19(17)25)28-27(31)32-15-24-22-10-3-1-8-20(22)21-9-2-4-11-23(21)24/h1-12,16,18,24H,13-15H2,(H,28,31)(H,29,30)/t18-/m0/s1

270063-46-2SDS

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-(S)-3-amino-4-(3-benzothienyl)-butyric acid

1.2 Other means of identification

Product number -
Other names FMOC-ALA(3-BZT)-(C*CH2)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:270063-46-2 SDS

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