71434-62-3

Basic information

• Product Name: Benzenemethanol, 4-bromo-a-pentyl-
• CAS NO: 71434-62-3
• Molecular Formula: C12H17BrO
• Molecular Weight: 257.17
• Mol File: 71434-62-3.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-bromo-a-pentyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-bromo-a-pentyl-(71434-62-3)
• EPA Substance Registry System: Benzenemethanol, 4-bromo-a-pentyl-(71434-62-3)

Safety Data

• Hazardous Substances Data: 71434-62-3(Hazardous Substances Data)

Upstream product

• 110-53-2 1-Bromopentane 
• 1122-91-4 4-bromo-benzaldehyde 
• 5391-88-8 1-(4-bromophenyl)ethanol 
• 71-36-3 butan-1-ol 
• 693-25-4 n-pentylmagnesium bromide 

Downstream Products

• 76287-58-6 1-Bromo-4-((E)-hex-1-enyl)-benzene 
• 836643-56-2 [1-(4-bromo-phenyl)-hexyloxy]-tert-butyl-dimethyl-silane 
• 910562-80-0 1-(4-bromo-phenyl)-hexan-1-ol 4-methoxybenzyl ether 
• 76287-45-1 Tris-(4-n-hexylphenyl)phosphin 
• 23703-22-2 1-bromo-4-n-hexylbenzene 
• 431041-25-7 (-)-(3aS,4S,5R,6aR)-5-hydroxy-4-{4-[(S)-1'-(tert-butyldimethylsilanyloxy)hexyl]phenyl}-5-[tert-butyldimethylsilanyloxy]hexahydropentalen-2-one 
• 431041-23-5 (+)-(3'aS,4'S,5'R,6'aR)-[4'-[4-((S)-1''-(tert-butyldimethylsilanyloxy)hexyl)phenyl]-1',6'a,6',3'a-tetrahydro-5,5-dimethylspiro[1,3-dioxane-2,2']]pentalen-5'-ol 
• 431041-21-3 (-)-[(S)-1-(4-bromophenyl)hexyloxy]tert-butyldimethylsilane 
• 431041-28-0 (-)-(S)-1-p-bromophenyl-1-hexanol 
• 7295-46-7 1-(4-bromophenyl)-1-hexanone 

Relevant articles and documents

Ruthenium-catalyzed β-alkylation of secondary alcohols with primary alcohols

The catalytic properties of a series of ruthenium complexes for β-alkylation of secondary alcohols with primary alcohols were studied. The catalytic activities of the ruthenium complexes were found to be dependent on the auxiliary ligands. The most active catalytic precursor found in this study is the ruthenium complex RuCl2(PPh3)2(2-NH2CH2Py) [2-NH2CH2Py = 2-aminomethyl pyridine], which effectively catalyzed the β-alkylation of both aryl- and alkyl-substituted secondary alcohols with benzylic and alkyl primary alcohols.

THERAPEUTIC SUBSTITUTED CYCLOPENTANES

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