109004-13-9

Basic information

• Product Name: [4-(p-toluenesulfonyloxymethyl)cyclohexyl]methanol
• Synonyms: [4-(p-toluenesulfonyloxymethyl)cyclohexyl]methanol
• CAS NO: 109004-13-9
• Molecular Weight: 298.403
• Mol File: 109004-13-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [4-(p-toluenesulfonyloxymethyl)cyclohexyl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(p-toluenesulfonyloxymethyl)cyclohexyl]methanol(109004-13-9)
• EPA Substance Registry System: [4-(p-toluenesulfonyloxymethyl)cyclohexyl]methanol(109004-13-9)

Safety Data

• Hazardous Substances Data: 109004-13-9(Hazardous Substances Data)

Upstream product

• 105-08-8 bis-1,4-(hydroxymethyl)cyclohexane 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1043911-56-3 [4-(azidomethyl)cyclohexyl]methanol 
• 4331-54-8 4-methylcyclohexanecarboxylic acid 
• 33242-79-4 4-methylcyclohexanecarbaldehyde 
• 34885-03-5 (4-methylcyclohexyl)methanol 
• 1097630-19-7 trans-1-ethynyl-4-(3,3,3-trifluoropropylsulfinylmethyl)cyclohexane 
• 1097630-17-5 trans-1-ethynyl-4-(3,3,3-trifluoropropylthiomethyl)cyclohexane 
• 1097630-16-4 trans-1-(2,2-dibromovinyl)-4-(3,3,3-trifluoropropylthiomethyl)cyclohexane 
• 1097630-14-2 trans-4-(3,3,3-trifluoropropylthiomethyl)cyclohexanecarbaldehyde 
• 1097630-15-3 cis-4-(3,3,3-trifluoropropylthiomethyl)cyclohexanecarbaldehyde 
• 1097630-08-4 trans-1-ethynyl-4-(3,3,3-trifluoropropylsulfonylmethyl)cyclohexane 
• 1097630-07-3 trans-1-(2,2-dibromovinyl)-4-(3,3,3-trifluoropropylsulfonylmethyl)cyclohexane 
• 1097630-06-2 trans-4-(3,3,3-trifluoropropanesulfonylmethyl)cyclohexane carbaldehyde 
• 1097630-04-0 trans-4-(3,3,3-trifluoropropylsulfonylmethyl)cyclohexylmethanol 
• 1097630-05-1 cis-4-(3,3,3-trifluoropropylsulfonylmethyl)cyclohexylmethanol 

Relevant articles and documents

METHOD OF PRODUCING ETHER DIOL COMPOUND

A method for manufacturing an ester diol compound according to an aspect of the present invention can manufacture an ester diol compound in high yield, can effectively manufacture in high yield. Moreover, the ester diol compound manufactured according to

Functionalization of Saturated Hydrocarbons. Part 4. The Gif System for Selective Oxidation using Molecular Oxygen

Various systems for the selective oxidation of saturated hydrocarbons have been developed.These are based on the idea of an iron catalyst which is reduced by electron transfer and oxidized by molecular oxygen simultaneously in the presence of a source of protons.Four modifications of this system (the Gif system) have been devised of which the best (Gif IV) consists of an iron catalyst with metallic zinc as the reductant, acetic acid as the proton source and pyridine as the solvent.At room temperature, using oxygen or air, saturated hydrocarbons are oxidized selectively to ketones in isolated yields superior to those reported for comparable model systems.