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2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID, also known as o-methoxyphenylglycine, is a chemical compound with the formula C10H13NO4. It is a derivative of the amino acid glycine, featuring an additional phenyl ring with a methoxy group attached. 2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID is recognized for its potential as a building block in organic synthesis and pharmaceutical research, where it can act as a precursor to various biologically active molecules. Its unique structure endows it with pharmacological properties, making it a subject of interest for its potential therapeutic applications in treating pain, inflammation, and other medical conditions.

22976-68-7

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22976-68-7 Usage

Uses

Used in Pharmaceutical Research:
2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID is used as a building block in pharmaceutical research for its ability to serve as a precursor to various biologically active molecules. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, 2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID is utilized as a key intermediate, contributing to the creation of complex organic compounds that may have applications in various industries.
Used in Medical Treatments:
2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID is studied for its potential use in the treatment of pain and inflammation, among other medical conditions. Its pharmacological properties are of interest to researchers and pharmaceutical companies seeking new therapeutic agents.
Used in Drug Development:
As a compound with demonstrated potential pharmacological properties, 2-AMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID is used in drug development to explore its efficacy and safety in treating specific medical conditions, with the aim of bringing new treatments to market.

Check Digit Verification of cas no

The CAS Registry Mumber 22976-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,7 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 22976-68:
(7*2)+(6*2)+(5*9)+(4*7)+(3*6)+(2*6)+(1*8)=137
137 % 10 = 7
So 22976-68-7 is a valid CAS Registry Number.

22976-68-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names o-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:22976-68-7 SDS

22976-68-7Relevant academic research and scientific papers

Bio-inspired enantioselective full transamination using readily available cyclodextrin

Zhang, Shiqi,Li, Guangxun,Liu, Hongxin,Wang, Yingwei,Cao, Yuan,Zhao, Gang,Tang, Zhuo

, p. 4203 - 4208 (2017/02/05)

The mimics of vitamin B6-dependent enzymes that catalyzed an enantioselective full transamination in the pure aqueous phase have been realized for the first time through the establishment of a new “pyridoxal 5′-phosphate (PLP) catalyzed non-covalent cyclodextrin (CD)-keto acid inclusion complexes” system, and various optically active amino acids have been obtained.

Synthesis of chirally pure 2,5-disubstituted diketopiperazines derived from trisubstituted phenylalanines

Danthi, Satyavijayan Narasimhan,Hill, Ronald A.

, p. 835 - 844 (2007/10/03)

Some new chirally pure 2,5-substituted diketopiperazines were synthesized starting from 2-methoxybenzyl alcohol. This multistep synthesis proceeds through the enzymatic synthesis of chirally pure amino acids, protection and dipeptide coupling, cyclization of dipeptide ester formates, and nitration of the resulting diketopiperazines.

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