368423-20-5

Basic information

• Product Name: Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3S)-rel- (9CI)
• Synonyms: Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3S)-rel- (9CI)
• CAS NO: 368423-20-5
• Molecular Formula: C10H15NO
• Molecular Weight: 165.2322
• Product Categories: ACETYLGROUP
• Mol File: 368423-20-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3S)-rel- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3S)-rel- (9CI)(368423-20-5)
• EPA Substance Registry System: Cyclobutaneacetonitrile, 3-acetyl-2,2-dimethyl-, (1R,3S)-rel- (9CI)(368423-20-5)

Safety Data

• Hazardous Substances Data: 368423-20-5(Hazardous Substances Data)

Upstream product

• 80-56-8 Pinene 
• 7785-26-4 (-)-α-pinene 
• 131488-84-1 2-morpholinopinan-3-one oxime 
• 7785-70-8 (+)-α-pinene 
• 546-67-8 lead(IV) tetraacetate 

Relevant articles and documents

Radical Fragmentation of β-Hydroxy Azides. Synthesis of Chiral Nitriles

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Transformation of peroxide products of olefin ozonolysis under treatment with hydroxylamine and semicarbazide hydrochlorides in acetic acid

Hydrochlorides of hydroxylamine and semicarbazide efficiently reduce peroxide products of olefin ozonolysis in a system CH2Cl2-AcOH leading to the formation of carboxylic acids and their derivatives. The application of water as the solvent component favors the increase in the fraction of nitrogen-containing organic compounds (semicarbazones, keto- and aldoximes, nitriles) and reduction in the yield of carboxylic acids.

Synthesis of highly functionalized chiral nitriles by radical fragmentation of β-hydroxy azides. Convenient transformation of aldononitriles into 1,4- and 1,5-iminoalditols

The synthesis of highly functionalized nitriles by an alkoxyl radical fragmentation of cyclic β-hydroxy azides is described. The alkoxyl radicals were generated by reaction of the alcohols with (diacetoxyiodo)benzene and iodine under mild conditions compa