13423-22-8

Basic information

• Product Name: 2-Azetidinone, 3,3,4,4-tetramethyl-
• Synonyms: 2-Azetidinone, 3,3,4,4-tetramethyl-;3,3,4,4-Tetramethylazetidin-2-one
• CAS NO: 13423-22-8
• Molecular Formula: C₇H₁₃NO
• Molecular Weight: 0
• Mol File: 13423-22-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Azetidinone, 3,3,4,4-tetramethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Azetidinone, 3,3,4,4-tetramethyl-(13423-22-8)
• EPA Substance Registry System: 2-Azetidinone, 3,3,4,4-tetramethyl-(13423-22-8)

Safety Data

• Hazardous Substances Data: 13423-22-8(Hazardous Substances Data)

Usage

General Description

2-Azetidinone, 3,3,4,4-tetramethyl- is a chemical compound with the molecular formula C8H15NO. Also known as N-tert-butyl-2-azetidinone, it is a white to off-white crystalline powder that is soluble in organic solvents. 2-Azetidinone, 3,3,4,4-tetramethyl- is primarily used as a building block and intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also utilized in the production of polymers and as a chiral auxiliary in organic synthesis. Additionally, 2-Azetidinone, 3,3,4,4-tetramethyl- has applications as an intermediate in the synthesis of various compounds for research and development purposes. While it has been identified as a potential skin and eye irritant, its specific hazards and safety considerations should be determined based on the specific application and handling conditions.

Upstream product

• 1189-71-5 isocyanate de chlorosulfonyle 
• 563-79-1 2,3-Dimethyl-2-butene 
• 17060-95-6 1-chlorosulfonyl-3,3,4,4-tetramethyl-2-azetidinone 

Downstream Products

• 22607-03-0 1-benzyl-3,3,4,4-tetramethylazetidin-2-one 
• 90886-53-6 2,2,3,3-Tetramethyl-β-alanin-methylester 
• 128694-06-4 5-Ethoxy-6,6,7,7-tetramethyl-2,4-bis-(4-nitro-phenyl)-1,3,4-triaza-bicyclo[3.2.0]hept-2-ene 
• 128694-05-3 2-(4-Chloro-phenyl)-5-ethoxy-6,6,7,7-tetramethyl-4-(4-nitro-phenyl)-1,3,4-triaza-bicyclo[3.2.0]hept-2-ene 
• 128694-10-0 5-Ethylsulfanyl-6,6,7,7-tetramethyl-4-(4-nitro-phenyl)-1,3,4-triaza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid methyl ester 
• 128694-08-6 5-(ethylthio)-4-(p-nitrophenyl)-2-phenyl-6,6,7,7-tetramethyl-1,3,4-triazabicyclo<3.2.0>hept-2-ene 
• 128694-04-2 5-ethoxy-4-(p-nitrophenyl)-2-phenyl-6,6,7,7-tetramethyl-1,3,4-triazabicyclo<3.2.0>hept-2-ene 
• 128694-03-1 1-(4-Nitro-phenyl)-5-(1,1,2-trimethyl-allyl)-1H-[1,2,4]triazole-3-carboxylic acid methyl ester 
• 128694-01-9 5-(2,3-dimethylbut-1-ene-3-yl)-1-(4-nitrophenyl)-3-phenyl-1,2,4-triazole 
• 128694-21-3 5-Ethylsulfanyl-6,6,7,7-tetramethyl-2-(2-nitro-phenyl)-4-oxa-1,3-diaza-bicyclo[3.2.0]hept-2-ene 
• 128694-18-8 5-Ethoxy-6,6,7,7-tetramethyl-2-(2-nitro-phenyl)-4-oxa-1,3-diaza-bicyclo[3.2.0]hept-2-ene 
• 128694-16-6 5-Ethoxy-2-(4-methoxy-phenyl)-6,6,7,7-tetramethyl-4-oxa-1,3-diaza-bicyclo[3.2.0]hept-2-ene 
• 128694-20-2 2-Phenyl-5-ethylthio-6,6,7,7-tetramethyl-4-oxa-1,3-diazabicyclo[3.2.0]hept-2-ene 
• 128694-17-7 5-Ethoxy-6,6,7,7-tetramethyl-2-phenyl-4-oxa-1,3-diaza-bicyclo[3.2.0]hept-2-ene 

Relevant articles and documents

A New Approach Using Aromatic-Solvent-Induced Shifts in NMR Spectroscopy to Analyze β-Lactams with Various Substitution Patterns

The chemical shifts of protons depend not only on the properties of the solute molecule but also on the medium in which the solute resides. A series of β-lactams with various substitution patterns were synthesized to study aromatic-solvent-induced shifts

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