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2-AMINO-3-(3-METHOXY-PHENYL)-PROPIONIC ACID, also known as homophenylalanine, is a non-proteinogenic amino acid characterized by its chemical structure that includes an amino group, a carboxylic acid group, and a side chain with a 3-methoxy-phenyl group. It serves as a crucial building block in the synthesis of peptides and proteins and has garnered interest for its potential therapeutic applications in neuroscience and pharmaceuticals. Homophenylalanine's ability to inhibit enzymes involved in neurotransmitter biosynthesis positions it as a promising drug target for conditions associated with neurotransmitter imbalances.

7635-28-1

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7635-28-1 Usage

Uses

Used in Pharmaceutical Industry:
2-AMINO-3-(3-METHOXY-PHENYL)-PROPIONIC ACID is used as a building block for the synthesis of peptides and proteins, contributing to the development of novel therapeutic agents. Its role in inhibiting enzymes involved in neurotransmitter biosynthesis makes it a potential drug target for conditions related to neurotransmitter imbalances, such as neurological disorders.
Used in Neuroscience Research:
In the field of neuroscience, 2-AMINO-3-(3-METHOXY-PHENYL)-PROPIONIC ACID is utilized for its potential therapeutic applications, particularly in the study and treatment of neurological disorders. Its ability to modulate neurotransmitter levels and influence enzyme activities involved in neurotransmitter biosynthesis offers a promising avenue for developing new treatments and understanding the underlying mechanisms of these conditions.
Used in Drug Discovery and Development:
2-AMINO-3-(3-METHOXY-PHENYL)-PROPIONIC ACID is employed as a key component in drug discovery and development processes. Its unique chemical structure and functional properties make it a valuable candidate for the design and synthesis of new pharmaceutical compounds with potential applications in various therapeutic areas, including the treatment of neurological disorders and other conditions related to neurotransmitter imbalances.

Check Digit Verification of cas no

The CAS Registry Mumber 7635-28-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,3 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7635-28:
(6*7)+(5*6)+(4*3)+(3*5)+(2*2)+(1*8)=111
111 % 10 = 1
So 7635-28-1 is a valid CAS Registry Number.

7635-28-1SDS

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 2-amino-3-(3-methoxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names m-Methoxy-phenylalanin

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:7635-28-1 SDS

7635-28-1Relevant academic research and scientific papers

Alkylation of N′-[(S)-1′-phenylethyl]-N-(diphenylmethylene)glycinamide using a phase transfer catalyst (PTC) for practical asymmetric syntheses of α-amino acid derivatives

Kim, Hyun Ju,Lee, Sang-Kuk,Park, Yong Sun

, p. 613 - 616 (2007/10/03)

The chiral auxiliary mediated stereoselective alkylation reaction of N′-[(S)-1′-phenylethyl]-N-(diphenylmethylene)glycinamide (1) using a phase transfer catalyst (PTC) is described. Alkylation of 1 using 18-crown-6 as a PTC for liquid-solid extraction of KOH in toluene gives best results. This methodology provides a practical protocol for the preparation of a variety of enantio-enriched unnatural α-amino acid derivatives up to 83:17 enantiomeric ratio.

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