213018-92-9 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-(+)-2-Chlorophenylglycine methyl ester hydrochloride is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Research and Development:
In research and development settings, (S)-(+)-2-CHLOROPHENYLGLYCINE METHYL ESTER HYDROCHLORIDE is used as a research tool for studying the activity and function of glutamate receptors. Its ability to bind and modulate these receptors makes it a valuable asset in understanding the underlying mechanisms of neurological disorders and developing potential treatments.
Used in Neurological Disorder Treatment:
(S)-(+)-2-Chlorophenylglycine methyl ester hydrochloride is being studied for its potential therapeutic applications in treating neurological disorders. Its interaction with glutamate receptors suggests that it may have a role in managing conditions related to neurotransmitter imbalances or receptor dysfunction.
Used in Mechanism of Disease Understanding:
As a compound that modulates glutamate receptor activity, (S)-(+)-2-CHLOROPHENYLGLYCINE METHYL ESTER HYDROCHLORIDE is used in laboratories to explore the mechanisms of diseases related to neurotransmission. This can lead to a better understanding of the pathophysiology of various neurological conditions and contribute to the development of targeted therapies.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 213018-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,0,1 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213018-92:
(8*2)+(7*1)+(6*3)+(5*0)+(4*1)+(3*8)+(2*9)+(1*2)=89
89 % 10 = 9
So 213018-92-9 is a valid CAS Registry Number.
213018-92-9Relevant academic research and scientific papers
Preparation method of (S)-chlorophenylglycine methyl ester hydrochloride
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Paragraph 0005; 0006; 0007; 0008, (2017/08/29)
The invention discloses a preparation method of (S)-chlorophenylglycine methyl ester hydrochloride. The preparation method comprises the following steps: 1) adding a mixture of o-chlorobenzaldehyde and trimethylsilyl cyanide into a reaction flask, then ad
Method for preparing 2-thienylethylamine derivatives
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, (2008/06/13)
PCT No. PCT/FR98/00441 Sec. 371 Date Sep. 2, 1999 Sec. 102(e) Date Sep. 2, 1999 PCT Filed Mar. 5, 1998 PCT Pub. No. WO98/39322 PCT Pub. Date Sep. 11, 1998The present invention relates to a process for the preparation of 2-thienylethylamine derivatives of general formula: as well as their acid addition salts, in which R represents a halogen atom and R1 represents a C1-C4 alkyl group, characterized in that a thienylglycidic derivative of general formula: in which M represents an alkali metal atom or a fraction of an alkaline-earth metal atom, is reacted with a phenylglycine ester, optionally in the form of a strong acid salt, of general formula: in which R and R1 have the same meaning as above, in the presence of an alkali metal borchydride of general formula: X-YIV in which X represents an alkali metal atom and Y represents a group of formula: -BH3CN or -BH(4-w)Zw in which Z represents a carboxylic acid residue and optionally in the presence of a C1-C4 carboxylic acid, which gives the desired compound in the form of a free base which can be treated, if necessary, with an acid in order to obtain an addition salt of this compound.
