60827-77-2

Basic information

• Product Name: (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine
• Synonyms: (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine
• CAS NO: 60827-77-2
• Molecular Weight: 315.326
• Mol File: 60827-77-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine(60827-77-2)
• EPA Substance Registry System: (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine(60827-77-2)

Safety Data

• Hazardous Substances Data: 60827-77-2(Hazardous Substances Data)

Usage

Description

(R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine is a chemical compound that serves as a crucial building block in the synthesis of various peptides and peptidomimetics. It is characterized by its role as a precursor in the preparation of protease inhibitors and enzyme activators, which are essential for the development of new drugs and therapeutic agents. (R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine is also recognized for its potential applications in the study of protein structure and function, making it a valuable tool for researchers in the fields of biochemistry and molecular biology.

Uses

Used in Pharmaceutical Industry:
(R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine is used as a precursor for the synthesis of protease inhibitors and enzyme activators for the development of new drugs and therapeutic agents. Its ability to modify and enhance the properties of peptides contributes to the advancement of pharmaceutical research and drug discovery.
Used in Biochemistry and Molecular Biology Research:
(R)-(N-benzyloxycarbonyl)-p-methoxyphenylglycine is used as a valuable tool for studying protein structure and function. Its application in this field aids researchers in understanding the complex interactions and mechanisms of proteins, which is crucial for the development of targeted therapies and the advancement of biomedical knowledge.

Upstream product

• 2540-53-6 2-(4-methoxyphenyl)glycine 
• 394210-44-7 4-(4-methoxy-phenyl)-2,5-dioxo-oxazolidine-3-carboxylic acid benzyl ester 

Downstream Products

• 736186-40-6 2-amino-2-(4-methoxy-phenyl)-N-phenyl-acetamide 
• 67412-96-8 D-(-)-4-methoxyphenylglycine amide 

Relevant articles and documents

Asymmetric synthesis of α-amino acids via cinchona alkaloid-catalyzed kinetic resolution of urethane-protected α-amino acid N-carboxyanhydrides

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