65392-83-8

Basic information

• Product Name: 3-(pentan-2-yl)phenol
• Synonyms: 3-(pentan-2-yl)phenol
• CAS NO: 65392-83-8
• Molecular Weight: 164.247
• Mol File: 65392-83-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(pentan-2-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(pentan-2-yl)phenol(65392-83-8)
• EPA Substance Registry System: 3-(pentan-2-yl)phenol(65392-83-8)

Safety Data

• Hazardous Substances Data: 65392-83-8(Hazardous Substances Data)

Upstream product

• 107-81-3 2-bromopentane 
• 4783-68-0 2-phenoxypyridine 
• 97218-43-4 3-(1-ethylpropyl)phenol 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 

Downstream Products

• 97218-43-4 3-(1-ethylpropyl)phenol 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 
• 60309-25-3 Butyl-carbamic acid 3-(1-methyl-butyl)-phenyl ester 
• 60309-23-1 Ethyl-carbamic acid 3-(1-methyl-butyl)-phenyl ester 
• 60309-24-2 Propyl-carbamic acid 3-(1-methyl-butyl)-phenyl ester 

Relevant articles and documents

Synthesis of m-Alkylphenols via a Ruthenium-Catalyzed C-H Bond Functionalization of Phenol Derivatives

The first example of the synthesis of m-alkylphenols via a ruthenium-catalyzed CAr-H bond functionalization of phenol derivatives with sec/tert-alkyl bromides is reported. Mechanistic studies indicated that the m-CAr-H bond alkylation may involve a radical process and that a six-membered ruthenacycle complex was the active catalyst. Moreover, this approach can provide an expedited strategy for the atom-/step-economical synthesis of many noteworthy pharmaceuticals and other functional molecules.

EQUILIBRIUM OF POSITIONAL ISOMERIZATION OF SECONDARY ALKYLBENZENES AND THEIR FUNCTIONAL DERIVATIVES

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