640768-72-5

Basic information

• Product Name: Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI)
• Synonyms: Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI);N-Methoxy-N-MethylcyclobutanecarboxaMide
• CAS NO: 640768-72-5
• Molecular Formula: C₇H₁₃NO₂
• Molecular Weight: 143.18362
• Product Categories: AMIDE
• Mol File: 640768-72-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 176.8±23.0 °C(Predicted)
• Appearance: /
• Density: 1.081±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI)(640768-72-5)
• EPA Substance Registry System: Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI)(640768-72-5)

Safety Data

• Hazardous Substances Data: 640768-72-5(Hazardous Substances Data)

Usage

General Description

Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI) is a chemical compound with the molecular formula C7H13NO2. It is a derivative of cyclobutanecarboxamide and is characterized by the presence of a methoxy and methyl group. Cyclobutanecarboxamide, N-methoxy-N-methyl- (9CI) may have applications in pharmaceutical and chemical synthesis due to its unique structure. Its properties and potential uses may make it of interest for further study and research.

Upstream product

• 1117-97-1 N,0-dimethylhydroxylamine 
• 5006-22-4 Cyclobutanecarbonyl chloride 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 3721-95-7 Cyclobutanecarboxylic acid 
• 765-85-5 methyl cyclobutanecarboxylate 

Relevant articles and documents

PYRROLOPYRIMIDINE ITK INHIBITORS

Disclosed herein are arylpyridinone compounds and compositions useful in the treatment of ITK mediated diseases, such as inflammation, having the structures of Formulas (I)-(IV): wherein the R groups, m, n, and X are as defined in the detailed description. Methods of inhibition of ITK activity in a human or animal subject are also provided.

Zn-ProPhenol Catalyzed Enantioselective Mannich Reaction of 2 H-Azirines with Alkynyl Ketones

The enantioselective Mannich reaction of 2H-azirines with alkynyl ketones is achieved under Zn-ProPhenol catalysis, delivering various aziridines with vicinal tetrasubstituted stereocenters in high yields with excellent enantioselectivities. The bimetalli

A C-H Insertion Approach to Functionalized Cyclopentenones

Cyclopentenones are synthetically versatile structures, and their straightforward construction from alkynone substrates by employing synthetically streamlining C-H insertion is conceptually appealing and of high synthetic potential. But, its implementation is very limited. Herein we report a Au-catalyzed version, which affords 2-bromocyclopent-2-en-1-ones with a broad scope and synthetically desirable diastereoselectivities. The proposed key intermediate capable of the observed insertion into unactivated C-H bonds is a fully functionalized gold vinylidene, which is generated via a novel intermolecular strategy. This flexible access of likely gold vinylidenes opens various opportunities to explore their versatile reactivities.