77651-55-9 Usage
Description
2-Methoxy phenylglycine methyl ester is a chemical compound that belongs to the family of phenylglycine derivatives. It is a methyl ester of 2-methoxy phenylglycine, characterized by a molecular formula of C10H13NO3 and a molecular weight of 195.21 g/mol. This white to off-white crystalline powder has a melting point of approximately 84-86°C and is frequently utilized as an intermediate in the synthesis of pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Industry:
2-Methoxy phenylglycine methyl ester is used as an intermediate in the synthesis of various pharmaceuticals for the treatment of diseases and disorders. Its versatile chemical structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Organic Compounds Synthesis:
In addition to its pharmaceutical applications, 2-methoxy phenylglycine methyl ester is also used as an intermediate in the synthesis of other organic compounds. Its unique properties make it a valuable building block for creating a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 77651-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,5 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77651-55:
(7*7)+(6*7)+(5*6)+(4*5)+(3*1)+(2*5)+(1*5)=159
159 % 10 = 9
So 77651-55-9 is a valid CAS Registry Number.
77651-55-9Relevant articles and documents
Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine
Inada, Haruki,Shibuya, Masatoshi,Yamamoto, Yoshihiko
, p. 11047 - 11059 (2020/10/12)
The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate the use of commercially available l-2-(2-chlorophenyl)glycine as the nitrogen source in the transamination of arylglyoxylic acids, producing the corresponding 2-arylglycines without interference from the undesired self-transamination process.
SYNTHESIS OF 2,3-BENZO-1-OXAOCTEM-4-CARBOXYLIC ACID
Daum, S. J.,Hansen, P. E.
, p. 1 - 6 (2007/10/02)
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