103889-81-2 Usage
Uses
Used in Organic Synthesis:
(S)-(o-Methoxyphenyl)glycine hydrochloride is used as a chiral auxiliary for controlling the stereochemistry of reactions in organic synthesis. Its application reason is to facilitate the creation of specific enantiomers, which are crucial in the development of pharmaceuticals and agrochemicals with desired biological activities.
Used in Pharmaceutical Preparation:
(S)-(o-Methoxyphenyl)glycine hydrochloride is used as a key component in the preparation of various pharmaceuticals. Its application reason is to provide a stable and easily handled form of the compound, which can be incorporated into the synthesis of drugs with specific therapeutic properties.
Used in Agrochemical Synthesis:
(S)-(o-Methoxyphenyl)glycine hydrochloride is also used in the preparation of agrochemicals. Its application reason is to aid in the development of compounds with targeted biological activities, such as pesticides or herbicides, that can be used in the agricultural industry to improve crop yield and protect plants from pests.
Check Digit Verification of cas no
The CAS Registry Mumber 103889-81-2 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, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103889-81:
(8*1)+(7*0)+(6*3)+(5*8)+(4*8)+(3*9)+(2*8)+(1*1)=142
142 % 10 = 2
So 103889-81-2 is a valid CAS Registry Number.
103889-81-2Relevant academic research and scientific papers
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.
