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103889-79-8

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103889-79-8 Usage

General Description

The chemical (R)-2-amino-2-(2-methoxyphenyl)acetic acid hydrochloride, also known as (R)-2-amino-2-(o-methoxyphenyl)acetic acid hydrochloride, is a compound used in the synthesis and study of pharmaceuticals and other organic compounds. It is an amino acid derivative with a hydrochloride salt form, and is classified as a chiral compound due to its asymmetric carbon center. This chemical has potential applications in the development of pharmaceutical drugs, research into biological processes, and as a building block for the synthesis of other organic molecules. Its properties and structure make it a valuable tool for researchers in various fields of chemistry and biology.

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.

103889-79-8Downstream Products

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.

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