103889-79-8 Usage
Description
(R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride, also known as (R)-2-amino-2-(o-methoxyphenyl)acetic acid hydrochloride, is a chiral compound that serves as an amino acid derivative in its hydrochloride salt form. It is characterized by an asymmetric carbon center, which makes it a valuable tool in the synthesis and study of pharmaceuticals and other organic compounds. This chemical is instrumental in the development of pharmaceutical drugs, research into biological processes, and as a building block for the synthesis of other organic molecules, making it a significant asset for researchers in the fields of chemistry and biology.
Uses
Used in Pharmaceutical Development:
(R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride is used as an intermediate in the synthesis of pharmaceutical drugs for its unique structural properties that can be leveraged to create novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, (R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride is used as a building block for the synthesis of other complex organic molecules, contributing to the creation of new compounds with potential applications in various industries.
Used in Biological Research:
(R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride is utilized in biological research as a chiral compound to study enzyme selectivity, receptor binding, and other biological processes that are sensitive to the stereochemistry of molecules.
Used in Chiral Chemistry:
(R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride is used as a chiral reference standard in analytical chemistry for the determination of enantiomeric purity and the study of stereoselective reactions.
Used in Drug Discovery:
In drug discovery, (R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride is used as a lead compound for the development of new pharmaceutical entities, given its potential to interact with biological targets in a stereospecific manner.
Check Digit Verification of cas no
The CAS Registry Mumber 103889-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,8 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103889-79:
(8*1)+(7*0)+(6*3)+(5*8)+(4*8)+(3*9)+(2*7)+(1*9)=148
148 % 10 = 8
So 103889-79-8 is a valid CAS Registry Number.
103889-79-8Relevant articles and documents
Synthesis of Optically Active Arylglycines by Photolysis of Optically Active (β-Hydroxyamino) Carbene-Chromium(0) Complexes
Vernier, Jean-Michel,Hegedus, Louis S.,Miller, David B.
, p. 6914 - 6920 (2007/10/02)
Photolysis of chromium complexes having the optically active amino alcohol (1R,2S)-(-)- or (1S,2R)-(+)-2-amino-1,2-diphenylethanol as the amino group produced aryl-substituted oxazinones in good yield with reasonable diastereoselectivity.Facile separation of diastereoisomers followed by mild reductive cleavage produced several arylglycines, having either electron-donating or withdrawing groups on the aromatic ring, in good overall yield and with excellent enantiomeric excess.
