114129-78-1

Basic information

• Product Name: Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5ba)]- (9CI)
• Synonyms: Cyclohexanone,5-methyl-2-(1-methylethyl)-,oxime,[2S-(1Z,2alpha,5bta)]-(9CI);Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5ba)]- (9CI);Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5b
• CAS NO: 114129-78-1
• Molecular Formula: C₁₀H₁₉NO
• Molecular Weight: 169.26
• Product Categories: ISOPROPYL
• Mol File: 114129-78-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5ba)]- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5ba)]- (9CI)(114129-78-1)
• EPA Substance Registry System: Cyclohexanone, 5-methyl-2-(1-methylethyl)-, oxime, [2S-(1Z,2alpha,5ba)]- (9CI)(114129-78-1)

Safety Data

• Hazardous Substances Data: 114129-78-1(Hazardous Substances Data)

Upstream product

• 546-88-3 acetylhydroxamic acid 
• 10458-14-7 Menthone 
• 62338-23-2 (2-isopropyl-5-methylcyclohexyloxy)trimethylsilane 
• 72020-06-5 2-(2-isopropyl-5-methylcyclohexyloxy)tetrahydro-2H-pyran 
• 94827-79-9 3-Chlor-3-nitroso-1-methyl-4-isopropyl-cyclohexan 
• 75-24-1 trimethylaluminum 

Downstream Products

• 2216-54-8 (+/-)-isomenthylamine 
• 2437-39-0 2-isopropyl-5-methyl-phenylamine 
• 330476-05-6 [(C₆H₅)3PCH₂C₆H₅]⁽¹⁺⁾*[PtCl₅(NHC(C₂H₅)ONC(C₉H₁₈))]^(1-)=[(C₆H₅)3PCH₂C₆H₅][PtCl₅(NHC(C₂H₅)ONC(C₉H₁₈))] 
• 56022-42-5 p-menthan-3-ylidene-nitro-amine 
• 10458-14-7 Menthone 
• 120625-76-5 C₁₇H₂₂N₄O₆ 
• 13559-68-7 1-Acetoxy-1-nitroso-2-isopropyl-5-methyl-cyclohexan 
• 21411-81-4 2-isopropyl-5-methyl-cyclohexylamine 
• 89-83-8 thymol 
• 32531-52-5 3,7-dimethyloctanoic acid 

Relevant articles and documents

Tandem and Selective Conversion of Tetrahydropyranyl and Silyl Ethers to Oximes Catalyzed with Trichloroisocyanuric Acid

Direct and oxidative conversion of tetrahydropyranyl and silyl ethers to oximes is described using trichloroisocyanuric acid (TCCA) as a relatively stable and inexpensive oxidant surprisingly in a catalytic amount and hydroxylamine hydrochloride under solvent-free conditions. Oximes can be synthesized from these protected alcohols in the presence of some other functional groups with excellent chemoselectivity using the present tandem catalytic method.

LIQUID CHROMATOGRAPHIC RESOLUTION OF RACEMIC KETONES AS THEIR OXIME 3,5-DINITROPHENYL CARBAMATES ON A CHIRAL STATIONARY PHASE

Cyclic and acyclic chiral ketones have been resolved as their oxime 3,5-dinitrophenyl carbamates on a chiral stationary phase derived from (S)-1-(6,7-dimethyl-1-naphthyl)isobutylamine.