91405-03-7

Basic information

• Product Name: Cyclohexanemethanol, 4-(1,1-dimethylethyl)-1-(1-methylethenyl)-, cis-
• CAS NO: 91405-03-7
• Molecular Formula: C14H26O
• Molecular Weight: 210.36
• Mol File: 91405-03-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Cyclohexanemethanol, 4-(1,1-dimethylethyl)-1-(1-methylethenyl)-, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanemethanol, 4-(1,1-dimethylethyl)-1-(1-methylethenyl)-, cis-(91405-03-7)
• EPA Substance Registry System: Cyclohexanemethanol, 4-(1,1-dimethylethyl)-1-(1-methylethenyl)-, cis-(91405-03-7)

Safety Data

• Hazardous Substances Data: 91405-03-7(Hazardous Substances Data)

Upstream product

• 91405-07-1 4β-(tert-butyl)-1α-(1-hydroxy-1-methylethyl)cyclohexanecarbonitrile 
• 91405-02-6 4β-(tert-butyl)-1α-(1-methylvinyl)cyclohexanecarbonitrile 
• 111324-95-9 methanesulfonic acid 4-tert-butyl-cyclohexyl ester 
• 31865-37-9 cis/trans-4-tert-Butylcyclohexancarbonitril 
• 98-52-2 4-(1,1-dimethylethyl)-cyclohexanol 
• 91405-15-1 4β-(tert-butyl)-1α-(1-methylvinyl)cyclohexanecarbaldehyde 

Downstream Products

• 91405-09-3 4-β-(tert-butyl)-1α-isopropyl-cyclohexanemethanol 

Relevant articles and documents

Cob(I)alamin Differentiating Alkenes During Saturation

The olefins 2, 7, 11, and 19 have been reduced using catalytic amounts of cob(I)alamin(1(I)).During a slow saturation, the catalyst is able to differentiate the two diastereotopic faces of the endocyclic double bonds in 11 (t1/2 40 d) and 19 (t1/2 80 d, cf.Scheme 4).The substrates 2 (t1/2 1 h, cf.Scheme 2) and 7 (t1/2 4 h, cf.Scheme 3) are reduced much faster.A rationalization of the data can be obtained formulating tertiary alkylcobalamins as intermediates.Of the oxime 6 ( cf.Scheme 2) and the p-bromobenzoate 23 (cf.Scheme 5) the structures have been determined by X-ray analysis.