39155-38-9

Basic information

• Product Name: (4-methyl-3-cyclohexen-1-yl)methanol(SALTDATA: FREE)
• Synonyms: (4-methyl-3-cyclohexen-1-yl)methanol(SALTDATA: FREE);(1-methylcyclohex-1-en-4-yl)-methanol;(4-methyl-3-cyclohexen-1-yl)methanol
• CAS NO: 39155-38-9
• Molecular Formula: C₈H₁₄O
• Molecular Weight: 126.19616
• Mol File: 39155-38-9.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 183.4°C at 760 mmHg
• Flash Point: 73.4°C
• Appearance: /
• Density: 0.925g/cm³
• Vapor Pressure: 0.223mmHg at 25°C
• Refractive Index: 1.472
• PKA: 14.96±0.10(Predicted)
• CAS DataBase Reference: (4-methyl-3-cyclohexen-1-yl)methanol(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methyl-3-cyclohexen-1-yl)methanol(SALTDATA: FREE)(39155-38-9)
• EPA Substance Registry System: (4-methyl-3-cyclohexen-1-yl)methanol(SALTDATA: FREE)(39155-38-9)

Safety Data

• Hazardous Substances Data: 39155-38-9(Hazardous Substances Data)

Usage

Description

(4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is a chemical compound classified as an alcohol. It is a colorless liquid with a strong, pleasant odor, making it a versatile ingredient in various consumer products.

Uses

Used in Fragrance and Flavor Industry:
(4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a fragrance and flavoring agent for its strong, pleasant odor, enhancing the sensory experience of various consumer products.
Used in Perfume Production:
In the perfume industry, (4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a key ingredient to create unique and appealing scents, contributing to the overall composition and character of perfumes.
Used in Cosmetics and Personal Care Products:
(4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is utilized in the formulation of cosmetics and personal care products, where its pleasant odor and other properties can improve the product's appeal and effectiveness.
Used as a Preservative:
Due to its antimicrobial properties, (4-methyl-3-cyclohexen-1-yl)methanol (SALTDATA: FREE) is used as a preservative in certain products to prevent microbial growth and extend shelf life.

InChI:InChI=1/C8H14O/c1-7-2-4-8(6-9)5-3-7/h2,8-9H,3-6H2,1H3

Upstream product

• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 4342-60-3 4-methylcyclohex-3-enecarboxylic acid 
• 20292-15-3 4-methyl-cyclohex-3-enecarboxylic acid ethyl ester 
• 6493-79-4 methyl 4-methyl-3-cyclohexene-1-carboxylate 

Downstream Products

• 50552-15-3 1-Methyl-4-nitrosooxymethyl-cyclohexene 
• 3937-49-3 (trans-4-methylcyclohexyl)methanol 
• 3937-48-2 (cis-4-Methyl-cyclohexyl)-methanol 
• 7560-64-7 4-methyl-cyclohex-3-enecarbaldehyde 
• 53216-76-5 4-Methyl-3-cyclohexen-1-acetonitril 
• 7086-66-0 2-<(1RS)-4-methylcyclohex-3-enyl>acetic acid 
• 31929-13-2 4-ethynyl-1-methylcyclohexene 
• 73494-01-6 3-(4'-methylcyclohex-3'-en-1-yl)but-2-enyl bromide 
• 29837-07-8 (Z)-α-bisabolene 
• 25532-79-0 (E)‐α‐bisabolene 
• 15760-18-6 3-(4-methyl-3-cyclohexen-1-yl)-1-butanol 
• 70240-37-8 (Z)-3-(4-methyl-3-cyclohexen-1-yl)-2-buten-1-ol 
• 162132-39-0 1,1-dibromo-2-(4-methyl-3-cyclohexen-1-yl)ethene 
• 162132-41-4 methyl 3-(4-methyl-3-cyclohexen-1-yl)propynoate 

Relevant articles and documents

Compound and preparation method and application thereof

The invention discloses a compound as well as a preparation method and application thereof, and the structural formula of the compound is as shown in formula 1. The research finds that the compound provided by the invention can be applied to preparation o

Simple, chemoselective hydrogenation with thermodynamic stereocontrol

Few methods permit the hydrogenation of alkenes to a thermodynamically favored configuration when steric effects dictate the alternative trajectory of hydrogen delivery. Dissolving metal reduction achieves this control, but with extremely low functional group tolerance. Here we demonstrate a catalytic hydrogenation of alkenes that affords the thermodynamic alkane products with remarkably broad functional group compatibility and rapid reaction rates at standard temperature and pressure.

Active ray curable ink-jet composition, image forming method using the same, ink-jet recording apparatus, and triarylsulfonium salt compound

An active ray curable ink-jet ink composition comprising a photo-induced acid generating agent containing an onium salt which does not generate benzene under active ray radiation, and a photopolymerizable compound containing a compound having an oxetane ring in the molecule.