67130-96-5

Basic information

• Product Name: 4-(2-bromophenyl)-2-butanol
• Synonyms: 4-(2-bromophenyl)-2-butanol
• CAS NO: 67130-96-5
• Molecular Weight: 229.117
• Mol File: 67130-96-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(2-bromophenyl)-2-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-bromophenyl)-2-butanol(67130-96-5)
• EPA Substance Registry System: 4-(2-bromophenyl)-2-butanol(67130-96-5)

Safety Data

• Hazardous Substances Data: 67130-96-5(Hazardous Substances Data)

Upstream product

• 3506-68-1 4-(2-bromophenyl)-2-butanone 
• 72454-54-7 4-(2-bromophenyl)but-3-en-2-one 
• 6630-33-7 ortho-bromobenzaldehyde 
• 468082-55-5 trans-4-(2-bromophenyl)-3-buten-2-one 
• 1378939-10-6 (E)-4-(2-bromophenyl)but-3-en-2-ol 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 58380-12-4 <(2-bromophenyl)methyl>propanedicarboxylic acid 
• 52221-92-8 3-(2-bromo-phenyl)-propan-1-ol 
• 15115-58-9 3-(2-bromophenyl)propionic acid 
• 66192-11-8 diethyl 2-(2-bromobenzyl)propan-1,3-dioate 
• 64-17-5 ethanol 
• 2039-88-5 2-bromostyrene 
• 917-54-4 methyllithium 
• 107408-16-2 3-(o-bromophenyl)propanal 

Downstream Products

• 79044-18-1 4-(o-Bromophenyl)-2-bromobutane 
• 107408-53-7 5-Methylene-3-oxo-7-phenyl-2-(triphenyl-λ⁵-phosphanylidene)-heptanoic acid ethyl ester 
• 107408-52-6 4-(1-Methyl-indan-1-yl)-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-butyric acid ethyl ester 
• 107408-15-1 (Z)-7-(2-Bromo-phenyl)-5-methyl-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-hept-4-enoic acid ethyl ester 
• 107408-18-4 ethyl 7-(2-bromophenyl)-5-methyl-3-oxo-2-(triphenylphosphoranylidene)-4-heptenoate 
• 767-58-8 1-methylindane 
• 2344-70-9 1-phenyl-3-butanol 

Relevant articles and documents

Switchable asymmetric bio-epoxidation of α,β-unsaturated ketones

Efficient asymmetric bio-epoxidation of electron-deficient α,β-unsaturated ketones was realized via a tandem reduction-epoxidation-dehydrogenation cascade, which proceeds in a switchable manner to afford either chiral epoxy ketones or allylic epoxy alcoho

A reaction for sp3-sp3 C-C bond formation via cooperation of Lewis acid-promoted/Rh-catalyzed C-H bond activation

A new method for intermolecular sp3-sp3 C-C bond formation between primary aliphatic alcohol and olefin by use of a RhCl(PPh3)3 (cat.)/BF3·OEt2 (2.5 equiv)/BuBr (0.5 equiv)/toluene system was first disclosed, which possessed quite significant utilities for organic synthesis, especially for that of secondary alcohols. The most significant aspect is the discovery that rhodium-catalyzed C-H bond activation of alcohols is feasible under Lewis acid-promoted conditions. Copyright

Lithium-Halogen Exchange-Initiated Cyclization Reactions. 3. Intramolecular Conjugate Addition Reactions of Unsaturated Acylphosphoranes

The lithium-halogen exchange-initiated intramolecular conjugate addition reactions of some model unsaturated acylphosphoranes have been examined.The effects of halide type, chain length, and acceptor substitution pattern on the feasibility of ring construction were studied.The lithium-bromine exchange reactions in two 2-bromooaryl acceptors were found to be too slow, relative to competing side reactions, to allow practical carbocycle syntheses while 3-,4-,5-, and 6-membered carbocycles are formed in good to excellent yields from precursors that are vinyl and saturated primary iodides.Highly efficient intramolecular conjugate addition reactions to β,β-disubstituted acceptor units are possible, and intermediate anions from intramolecular conjugate addition reactions are readily captured with electrophiles.