31848-98-3

Basic information

• Product Name: Benzenemethanol, a-(4-chlorobutyl)-
• CAS NO: 31848-98-3
• Molecular Formula: C11H15ClO
• Molecular Weight: 198.692
• Mol File: 31848-98-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-(4-chlorobutyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(4-chlorobutyl)-(31848-98-3)
• EPA Substance Registry System: Benzenemethanol, a-(4-chlorobutyl)-(31848-98-3)

Safety Data

• Hazardous Substances Data: 31848-98-3(Hazardous Substances Data)

Upstream product

• 927-73-1 3-butenyl chloride 
• 100-52-7 benzaldehyde 
• 139527-25-6 bis(4-chlorobutyl)zinc 
• 100-58-3 phenylmagnesium bromide 
• 71-43-2 benzene 
• 1195776-84-1 1-methoxymethoxy-1-phenyl-5-chloropentane 
• 1575-61-7 5-Chlorovaleroyl chloride 
• 501-53-1 benzyl chloroformate 
• 22815-63-0 N-^t-butyl benzylcarbamate 
• 6940-78-9 4-chlorobutyl bromide 
• 20074-80-0 5-chloro-pentanal 
• 942-93-8 5-Chloro-1-phenyl-1-pentanone 

Downstream Products

• 942-93-8 5-Chloro-1-phenyl-1-pentanone 
• 4203-44-5 2-phenyltetrahydropyran 
• 123537-30-4 (S)-2-phenyltetrahydro-2H-pyran 
• 1554032-30-2 methyl 4-benzoyl-3-(4-methylphenyl)-4-pentenoate 
• 202325-96-0 1,5-dichloro-1-phenylpentane 
• 66534-77-8 3-phenyl-2,2-dimethylheptan-3-ol 
• 66860-64-8 5-iodo-1-phenyl-1-pentanone 
• 1009-14-9 phenyl butyl ketone 
• 10487-96-4 1-phenylcyclopentanol 
• 65002-76-8 N-(5-Dimethylamino-1-phenyl-pentyl)-benzamide 
• 1622-06-6 2-phenyl-tetrahydro-thiopyran 
• 176503-81-4 N-(5-Chloro-1-phenyl-pentyl)-benzamide 

Relevant articles and documents

Chemoselective lithiation of 1-Bromo-n-chloroalkanes

Reactions between different 1-bromo-n-chloroalkanes (1-3), lithium/naphthalene (1:2 molar ratio) and a carbonyl compound R 1R2CO in THF at -78°C provide, after hydrolysis with water, the corresponding chlorinated alcohols 4 through s

A combined computational and experimental investigation of the oxidative ring-opening of cyclic ethers by oxoammonium cations

The propensity of oxoammonium cations to facilitate the oxidative ring-opening of cyclic ethers to their corresponding distal hydroxy ketones is investigated. The reaction has been evaluated using experimental and computational methods to gain deeper insight into trends in reactivity.