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FMOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID is a chiral chemical compound belonging to the class of phenylpropanoic acids. It is a derivative of amino acids, characterized by the presence of an FMOC (9-fluorenylmethyloxycarbonyl) protecting group, which is commonly used in peptide synthesis. The (S) designation signifies the specific stereochemistry of the molecule, making it a versatile building block for the creation of various peptides in pharmaceutical and biochemical applications.

501015-27-6

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501015-27-6 Usage

Uses

Used in Pharmaceutical Industry:
FMOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID is used as a key intermediate in the synthesis of peptides and proteins for various therapeutic applications. Its chiral nature and the presence of the FMOC protecting group facilitate the controlled assembly of peptide sequences, enabling the development of novel drugs with improved efficacy and selectivity.
Used in Biochemical Research:
In the field of biochemistry, FMOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID serves as a valuable tool for studying protein structure, function, and interactions. Its unique chemical properties allow researchers to investigate the role of specific amino acid residues in protein folding, stability, and binding processes, contributing to a deeper understanding of biological systems.
Used in Peptide Synthesis:
FMOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID is used as a building block in the synthesis of custom peptides for various applications, including drug discovery, diagnostics, and therapeutics. Its versatility and the ease of incorporating the FMOC protecting group make it an ideal choice for constructing complex peptide sequences with precise control over their stereochemistry and functionality.
Used in Chemical Synthesis:
FMOC-(S)-3-AMINO-3-(3-METHYL-PHENYL)-PROPIONIC ACID is employed as a versatile chemical intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structural features and reactivity enable the development of novel synthetic routes and the production of high-value products with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 501015-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 501015-27:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*5)+(2*2)+(1*7)=76
76 % 10 = 6
So 501015-27-6 is a valid CAS Registry Number.

501015-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(3-methylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(m-tolyl)propanoic acid

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:501015-27-6 SDS

501015-27-6Upstream product

501015-27-6Downstream Products

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