106166-01-2

Basic information

• Product Name: (4-bromophenyl)-cyclohexyl methanol
• Synonyms: (4-bromophenyl)-cyclohexyl methanol
• CAS NO: 106166-01-2
• Molecular Weight: 269.181
• Mol File: 106166-01-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (4-bromophenyl)-cyclohexyl methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-bromophenyl)-cyclohexyl methanol(106166-01-2)
• EPA Substance Registry System: (4-bromophenyl)-cyclohexyl methanol(106166-01-2)

Safety Data

• Hazardous Substances Data: 106166-01-2(Hazardous Substances Data)

Upstream product

• 110-82-7 cyclohexane 
• 1122-91-4 4-bromo-benzaldehyde 
• 106-37-6 1.4-dibromobenzene 
• 2043-61-0 cyclohexanecarbaldehyde 
• 36140-19-9 dicyclohexylboron chloride 
• 931-51-1 cyclohexylmagnesiumchloride 
• 931-50-0 cyclohexylmagnesium bromide 

Downstream Products

• 3277-79-0 (4-bromophenyl)(cyclohexyl)methanone 
• 1158041-63-4 1-(4-bromophenyl)-1-cyclohexylethanol 
• 263257-26-7 cyclohexyl(4-(2-quinol-2-ylethenyl)phenyl)methanol O-tertbutyldimethylsilyl ether 
• 263256-92-4 cyclohexyl(4-(2-quinol-2-ylethyl)phenyl)methanol 
• 1027056-41-2 O-{cyclohexyl-[4-(2-quinolin-2-yl-ethyl)-phenyl]-methyl}-hydroxylamine 
• 263256-90-2 cyclohexyl(4-(2-quinol-2-ylethenyl)phenyl)methanol 
• 263256-89-9 cyclohexyl(4-formylphenyl)methanol tert-butyldimethylsilyl ether 
• 263257-25-6 (4-bromophenyl)cyclohexylmethanol O-tert-butyldimethylsilyl ether 

Relevant articles and documents

Coupling Reaction between Aldehydes and Non-Activated Hydrocarbons via the Reductive Radical-Polar Crossover Pathway

Herein, we describe the generation of an organochromium-type carbanion species from a non-activated C-H bond and its nucleophilic addition to aldehydes. The catalytic carbanion generation occurred through formal deprotonation of a non-activated C-H bond under mild conditions and did not need the prefunctionalization or anion stabilizing group. Carbon radical intermediates generated by decatungstate photocatalyst-mediated hydrogen abstraction were captured by a chromium salt with the reductive radical-polar crossover reaction to produce organochromium carbanions.

12-ARYL PROSTAGLANDIN ANALOGS

Compounds comprising the formula (I) are disclosed, wherein Y, A, X, R, D, and n are as described. A compound comprising a prostaglandin EP2 selective agonist wherein the ω-chain comprises a substituted phenyl, wherein at least one substituent

A new method for alkylation of aromatic aldehydes using alkylboron chloride derivatives in the presence of oxygen

Reactions of aromatic aldehydes with alkylboron chloride derivatives in the presence of oxygen have been investigated. Dialkylboron chlorides react with aryl aldehydes to produce arylalkylmethanols in good to excellent yields. Under the same reaction conditions, alkylboron dichlorides lead to the formation of arylalkyl chlorides.