17475-43-3

Basic information

• Product Name: Benzenemethanol, 2-propyl-
• CAS NO: 17475-43-3
• Molecular Formula: C10H14O
• Molecular Weight: 150.221
• Mol File: 17475-43-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-propyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-propyl-(17475-43-3)
• EPA Substance Registry System: Benzenemethanol, 2-propyl-(17475-43-3)

Safety Data

• Hazardous Substances Data: 17475-43-3(Hazardous Substances Data)

Upstream product

• 496-14-0 1,3-dihydroisobenzofuran 
• 74-96-4 ethyl bromide 
• 119-64-2 tetralin 
• 89-95-2 2-methyl-benzyl alcohol 
• 75-03-6 ethyl iodide 
• 89-71-4 2-Methyl-benzoic acid methyl ester 
• 1821-39-2 2-propylaniline 
• 19614-14-3 1-bromo-2-propylbenzene 

Downstream Products

• 1268267-69-1 1,3-dimethyl-5-(2-propylbenzylidene)pyrimidine-2,4,6(1H,3H,5H)-trione 
• 59059-44-8 o-propylbenzaldehyde 
• 103323-66-6 2-propyl-benzyl chloride 
• 17071-22-6 3,5-dinitro-benzoic acid-(2-propyl-benzyl ester) 
• 611-45-0 1-Benzyl-naphthalene 

Relevant articles and documents

Selective aerobic oxidation of alkyl aromatics on Bi2MoO6 nanoplates decorated with Pt nanoparticles under visible light irradiation

Pt/Bi2MoO6 nanoplates are efficient photocatalysts for the selective oxidation of saturated C-H bonds in alkyl aromatics under visible light illumination using O2 as an oxidant. This study opens a new window for direct C-H functionalization through the photocatalytic method based on cheap Bi2MoO6 semiconductor materials.

Expeditious construction of a carbobicyclic skeleton via sp3-C-H functionalization: Hydride shift from an aliphatic tertiary position in an internal redox process

Described herein is the first example of an aliphatic, nonbenzylic hydride shift/cyclization sequence that contains two types of novel sp3-C-H functionalization: (1) construction of a tetraline skeleton via [1,5]-hydride shift/cyclization and (2) [1,6]-hydride shift/cyclization to form a five-membered ring (indane derivatives).

Process for producing cyclopropanecarboxylates

There is disclosed a process process for producing a cyclopropanecarboxylate of formula (1): 1which process comprises reacting cyclopropanecarboxylic acid of formula (2): 2with a monohydroxy compound of formula (3): R6OH??(3),in the presence of a catalyst compound comprising an element of to Group 4 of the Periodic Table of Elements.