3236-47-3

Basic information

• Product Name: [4-(hydroxymethyl)cyclohexyl]methanol
• Synonyms: [4-(hydroxymethyl)cyclohexyl]methanol
• CAS NO: 3236-47-3
• Molecular Formula: C₈H₁₆O₂
• Molecular Weight: 144.21
• Mol File: 3236-47-3.mol
• Article Data: 13

Chemical Properties

• Melting Point: 42-43 °C
• Boiling Point: 286.229 °C at 760 mmHg
• Flash Point: 161.111 °C
• Appearance: /
• Density: 1.004 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.471
• PKA: 14.75±0.10(Predicted)
• CAS DataBase Reference: [4-(hydroxymethyl)cyclohexyl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [4-(hydroxymethyl)cyclohexyl]methanol(3236-47-3)
• EPA Substance Registry System: [4-(hydroxymethyl)cyclohexyl]methanol(3236-47-3)

Safety Data

• Hazardous Substances Data: 3236-47-3(Hazardous Substances Data)

Usage

General Description

[4-(hydroxymethyl)cyclohexyl]methanol is a chemical compound with the molecular formula C8H16O2. It is an aliphatic alcohol that contains a cyclohexyl ring with a hydroxymethyl group attached to it. [4-(hydroxymethyl)cyclohexyl]methanol is commonly used as a building block in organic synthesis and pharmaceutical manufacturing. It has applications in the production of fragrances, flavors, and other specialty chemicals. The hydroxymethyl group in this compound makes it a versatile building block for creating a variety of different compounds with diverse properties and uses. Additionally, it is a colorless liquid with a characteristic odor and is slightly soluble in water.

InChI:InChI=1/C8H16O2/c9-5-7-1-2-8(6-10)4-3-7/h7-10H,1-6H2/t7-,8+

Upstream product

• 3399-22-2 dimethyl 1,4-cyclohexanedicarboxylate 
• 3399-21-1 cis-dimethyl 1,4-cyclohexanedicarboxylate 
• 98837-34-4 ethyl 3-hydroxy-2-methylenebutanoate 
• 140-88-5 ethyl acrylate 
• 1420954-46-6 bis((4-methylcyclohexyl)methyl) cyclohexane-1,4-dicarboxylate 
• 95623-88-4 terephthalic acid 1,4-bis(4-methylcyclohexyl)methyl ester 
• 100-21-0 terephthalic acid 
• 619-81-8 cis-cyclohexane-1,4-dicarboxylic acid 
• 120-61-6 1,4-benzenedicarboxylic acid dimethyl ester 
• 108-05-4 vinyl acetate 
• 105-08-8 bis-1,4-(hydroxymethyl)cyclohexane 
• 116076-50-7 (1,4-cis-cyclohexanediyl)bis(methylene)dimethanesultonate 
• 3412-69-9 cis-1,4-cyclohexanedimethanol dibenzoate 
• 1119-43-3 (E,E)-hexa-2,4-dienedioic acid dimethyl ester 

Downstream Products

• 1187855-98-6 ((1s,4s)-4-(hydroxymethyl)cyclohexyl)methyl phenylcarbamate 
• 1187856-21-8 (cis-4-(hydroxymethyl)cyclohexyl)methyl diphenylcarbamate 
• 1187856-34-3 tert-butyl 2-(((1s,4s)-4-(hydroxymethyl)cyclohexyl)methoxy)acetate 
• 15898-77-8 (Z)-1,4-bis(bromomethyl)cyclohexane 
• 180046-56-4 tert-butyl (((1s,4s)-4-(cyanomethyl)cyclohexyl)methyl)carbamate 
• 1187856-33-2 2-((cis-4-((3,3-diphenylureido)methyl)cyclohexyl)methoxy)acetic acid 
• 1187856-35-4 tert-butyl 2-((cis-4-((methylsulfonyloxy)methyl)cyclohexyl)methoxy)acetate 

Relevant articles and documents

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The invention is directed to a process for preparing a 1,4-disubstituted cyclohexane compound of formula (I): where A is —OH, —OR, Br, or Cl; and R is a silyl group, a hydrocarbyl group, or an acyl group having 1 to 12 carbon atoms. The process includes the steps of reacting ethylene with a (2E,4E)-hexa-2,4-diene compound to produce a 3,6-disubstituted cyclohex-1-ene compound, and hydrogenating the 3,6-disubstituted cyclohex-1-ene compound to yield the 1,4-disubstituted cyclohexane compound of formula (I).