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878011-67-7

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878011-67-7 Usage

Description

(S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID, also known as (S)-4-(4-METHOXYPHENYL)-3-AMINOBUTANOIC ACID or (S)-HOMOPHENYLALANINE, is a non-proteinogenic amino acid with the molecular formula C11H15NO3. It is a chiral molecule with two enantiomers, where the (S)-enantiomer is the biologically active form. (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is often utilized in the synthesis of peptides and pharmaceuticals and has potential applications in treating various medical conditions. Additionally, it serves as a valuable tool in studying biological systems and drug development.

Uses

Used in Pharmaceutical Industry:
(S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its potential applications in treating various medical conditions. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Peptide Synthesis:
In the field of peptide synthesis, (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is used as a building block to create specific peptide sequences. Its incorporation into peptides can lead to the development of novel therapeutic agents with targeted biological activities.
Used in Biological Research:
(S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is used as a research tool in biological studies to investigate the mechanisms of various biological processes and to identify potential drug targets. Its chiral nature and biological activity make it an interesting subject for scientific exploration.
Used in Drug Development:
As a compound with potential therapeutic applications, (S)-3-AMINO-4-(4-METHOXYPHENYL)BUTANOIC ACID is used in drug development to design and test new pharmaceutical agents. Its unique properties and potential medical uses make it a promising candidate for the creation of innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 878011-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,0,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 878011-67:
(8*8)+(7*7)+(6*8)+(5*0)+(4*1)+(3*1)+(2*6)+(1*7)=187
187 % 10 = 7
So 878011-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-15-10-4-2-8(3-5-10)6-9(12)7-11(13)14/h2-5,9H,6-7,12H2,1H3,(H,13,14)/t9-/m0/s1

878011-67-7SDS

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-amino-4-(4-methoxyphenyl)butanoic acid

1.2 Other means of identification

Product number -
Other names benzenebutanoic acid,A'A|Afas-amino-4-methoxy-,(betaS)

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:878011-67-7 SDS

878011-67-7Upstream product

878011-67-7Downstream Products

878011-67-7Relevant articles and documents

A novel approach to homochiral β-amino acids 1

Seki, Masahiko,Matsumoto, Kazuo

, p. 3165 - 3168 (2007/10/03)

An efficient synthesis of γ-aryl or alkyl substituted β-amino acids starting from N-Cbz-L-homoserine lactone via the formation of α-amino aryl, alkenyl or alkynyl ketones with the original α-carbon chirality retained as such is described. Copyright

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