935764-11-7

Basic information

• Product Name: 2-(4-methoxyphenyl)-2-oxoacetamide
• Synonyms: 2-(4-methoxyphenyl)-2-oxoacetamide
• CAS NO: 935764-11-7
• Molecular Weight: 179.175
• Mol File: 935764-11-7.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxyphenyl)-2-oxoacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-2-oxoacetamide(935764-11-7)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-2-oxoacetamide(935764-11-7)

Safety Data

• Hazardous Substances Data: 935764-11-7(Hazardous Substances Data)

Upstream product

• 40140-16-7 ethyl (p-methoxyphenyl)oxoacetate 
• 19513-78-1 1-(4-methoxy-phenyl)-2-phenoxy-ethanone 
• 19513-80-5 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethan-1-one 
• 6832-17-3 2-diazo-1-(4-methoxyphenyl)ethanone 
• 104-47-2 p-methoxybenzylnitrile 
• 58125-69-2 ethyl 2-(4-methoxyphenyl)acetimidate hydrochloride 
• 18362-51-1 1,3-bis(4'-methoxyphenyl)propane-1,3-dione 
• 4648-54-8 trimethylsilylazide 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 7099-91-4 p-methoxybenzoylformic acid 
• 117177-66-9 2-(4-methoxyphenyl)-2-oxoacetyl chloride 
• 1218939-15-1 C₁₇H₂₅NO₃ 
• 100-07-2 4-methoxy-benzoyl chloride 
• 696-62-8 para-iodoanisole 

Downstream Products

• 144664-14-2 (S)-2-hydroxy-2-(4-methoxyphenyl)acetamide 
• 21165-16-2 (R)-2-hydroxy-2-(4-methoxyphenyl)acetamide 
• 27623-06-9 6-(4-methoxyphenyl)-3-thioxo-3,4-dihydro-1,2,4-triazin-5(2H)-one 
• 91121-61-8 2-hydroxy-2-(4-methoxy-phenyl)-propionic acid 
• 91121-61-8 2-(4-methoxyphenyl)-2-hydroxypropanoic acid 

Relevant articles and documents

Metabolically stable vanillin derivatives for the treatment of hypoxia

Vanillin derivative compounds that bind covalently with hemoglobin are provided. Methods of treating sickle cell disease and other hypoxia-related disorders by administering such compounds are also provided.

Oxidative Coupling of Diazo and NH4I: A Route to Primary Oxamates and α-Ketoamides

A simple and efficient method has been developed for the preparation of primary oxamates and α-ketoamides through the oxidative coupling of diazo compounds and NH4I. Under the optimized reaction conditions, a range of diazoesters and α-diazoketones was explored, and the corresponding products were obtained in moderate to good yields. This protocol is metal-free, is performed under mild conditions, has a wide substrate scope, and offers operational simplicity.

A room temperature next amine control lignin model molecular breaking method

The invention relates to a room temperature next amine control lignin model molecular breaking method. The method adopts the 1 - aryl - 2 - [...] as lignin β - O - 4 model molecule, in under the action of the copper salt and an amine, is oxidized and broken C - C/C - O key; wherein a primary and secondary aliphatic amine control into aromatic amide and a phenolic compound, inorganic ammonia control generating α - one amide and phenolic compound, tertiary amine control into aromatic acid and phenol compounds. The testing process are as follows: the 1 - aryl - 2 - [...], amine compound with a copper salt in dimethyl sulfoxide in mixed, put in the pressure container, the charge air or oxygen after the replacement is closed, at room temperature, stirring the reaction 8 - 12 is H, can occur model molecular C - C/C - O bond breaking, to obtain aromatic amide, α - one amide, aromatic acid and phenol compounds. The mild conditions, cheap catalyst and oxidizing agent, various controllable reaction product, the reaction process is simple and easy to operate.