62086-71-9

Basic information

• Product Name: Glycine, N-(4-methoxybenzoyl)-, methyl ester
• CAS NO: 62086-71-9
• Molecular Formula: C11H13NO4
• Molecular Weight: 223.229
• Mol File: 62086-71-9.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Glycine, N-(4-methoxybenzoyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(4-methoxybenzoyl)-, methyl ester(62086-71-9)
• EPA Substance Registry System: Glycine, N-(4-methoxybenzoyl)-, methyl ester(62086-71-9)

Safety Data

• Hazardous Substances Data: 62086-71-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 5680-79-5 glycine ethyl ester hydrochloride 
• 100-07-2 4-methoxy-benzoyl chloride 
• 616-34-2 methoxycarbonylmethylamine 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 28507-33-7 quinolin-8-yl-4-methoxybenzoate 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-09-4 4-methoxybenzoic acid 
• 150-13-0 4-amino-benzoic acid 

Downstream Products

• 2482-25-9 4-hydroxyhippuric acid 
• 743457-68-3 5-methoxy-2-(4-methoxyphenyl)thiazole 
• 67567-57-1 2-(p-methoxyphenyl)-5-methoxyoxazole 

Relevant articles and documents

Quinolin-8-yl Formate: A New Option for Small-Scale Carbonylation Reactions in Microwave Reactors

A convenient procedure for conducting small-scale carbonylations of aryl or benzyl halides in a microwave reactor by using quinolin-8-yl formate is described. The resulting 8-acyloxyquinolines were shown to be more reactive than phenyl esters in acyl-tran

Palladium-Catalyzed Oxidative Carbonylation of Aryl Hydrazines with CO and O2 at Atmospheric Pressure

Palladium-catalyzed aerobic oxidative aminocarbonylation and alkoxycarbonylation reactions with aryl hydrazines as coupling partners have been developed. The oxidative carbonylation of aryl hydrazines proceeded smoothly at atmospheric pressure CO, employi

Catalytic, asymmetric, and stereodivergent synthesis of non-symmetric β,β-Diaryl-α-Amino Acids

We report a concise, enantio- and diastereoselective route to novel nonsymmetrically substituted N-protected β,β-diaryl-α-amino acids and esters, through the asymmetric hydrogenation of tetrasubstituted olefins, some of the most challenging examples in the field. Stereoselective generation of an E- or Z-enol tosylate, when combined with stereoretentive Suzuki-Miyaura cross-coupling and enantioselective hydrogenation catalyzed by (NBD)2RhBF4 and a Josiphos ligand, allows for full control over the two vicinal stereogenic centers. High yields and excellent enantioselectivities (up to 99% ee) were obtained for a variety of N-acetyl, N-methoxycarbonyl, and N-Boc β,β-diaryldehydroamino acids, containing a diverse and previously unreported series of heterocyclic and aryl substituted groups (24 examples) and allowing access to all four stereoisomers of these valuable building blocks.