2808-76-6

Basic information

• Product Name: 1,3-DIMETHYLCYCLOHEXENE
• Synonyms: 1,3-Dimethyl-1-cyclohexene;Cyclohexene, 1,3-dimethyl-;cyclohexene,1,3-dimethyl-;1,3-DIMETHYLCYCLOHEXENE
• CAS NO: 2808-76-6
• Molecular Formula: C₈H₁₄
• Molecular Weight: 110.2
• Mol File: 2808-76-6.mol
• Article Data: 13

Chemical Properties

• Melting Point: -81.99°C (estimate)
• Boiling Point: 127.05°C
• Flash Point: 12.8°C
• Appearance: /
• Density: 0.7991
• Vapor Pressure: 14mmHg at 25°C
• Refractive Index: 1.4471
• CAS DataBase Reference: 1,3-DIMETHYLCYCLOHEXENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-DIMETHYLCYCLOHEXENE(2808-76-6)
• EPA Substance Registry System: 1,3-DIMETHYLCYCLOHEXENE(2808-76-6)

Safety Data

• Hazardous Substances Data: 2808-76-6(Hazardous Substances Data)

Usage

General Description

1,3-DIMETHYLCYCLOHEXENE is a colorless liquid aromatic compound with the chemical formula C8H14. It is a symmetrical isomer of 1,4-dimethylcyclohexene and is commonly used as a solvent in organic synthesis. This chemical is highly flammable and should be handled with caution. 1,3-DIMETHYLCYCLOHEXENE is commonly found in industrial settings where it is used as a raw material in the production of various chemicals, including pharmaceuticals, fragrances, and pesticides. It is also used in the manufacturing of rubber and plastics. Additionally, it is used in the production of adhesives and surfactants.

InChI:InChI=1/C8H14/c1-7-4-3-5-8(2)6-7/h6-7H,3-5H2,1-2H3

Upstream product

• 110-93-0 6-Methyl-hept-5-en-2-on 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 108-38-3 m-xylene 
• 7664-93-9 sulfuric acid 
• 87-62-7 2,6-dimethylaniline 
• 112-80-1 cis-Octadecenoic acid 
• 67-56-1 methanol 
• 24213-44-3 cis,cis-2,6-dimethylcyclohexylamine 
• 158362-89-1 1,3-dimethyl-2-iodo-cyclohex-1-ene 
• 19860-52-7 2,6-dimethylcyclohexyl acetate 
• 5337-72-4 2,6-dimethylcyclohexanol 
• 107-41-5 2-methyl-2,4-pentanediol 
• 74-85-1 ethene 
• 90255-42-8 2,6-dimethyl-1-cyclohexanone hydrazone 

Downstream Products

• 74964-49-1 (S)-2-Chloro-3-((1S,2S)-2-methyl-6-methylene-cyclohexyl)-propionic acid methyl ester 
• 74985-31-2 (S)-2-Chloro-3-((1S,2R)-2-methyl-6-methylene-cyclohexyl)-propionic acid methyl ester 
• 162239-52-3 1,5-Dimethyl-7-oxabicyclo[4.1.0] -heptane 
• 73650-09-6 (Z)-2-((1S,6S)-2,6-Dimethyl-cyclohex-2-enyl)-but-2-enedioic acid dimethyl ester 
• 73588-05-3 (Z)-2-((1S,6R)-2,6-Dimethyl-cyclohex-2-enyl)-but-2-enedioic acid dimethyl ester 
• 162239-52-3 1,3-dimethyl-cis-1,2-epoxycyclohexane 
• 162239-52-3 1,3-dimethyl-trans-1,2-epoxycyclohexane 
• 108-38-3 m-xylene 
• 638-04-0 1,3-dimethylcyclohexane 
• 62587-11-5 9-(2t,6t-dimethyl-cyclohex-r-yl)-9-bora-bicyclo[3.3.1]nonane 

Relevant articles and documents

Effect of ketene additive and Si/Al ratio on the reaction of methanol over HZSM-5 catalysts

The influence of ketene as possible intermediate for the reaction of methanol to aromatics was investigated over HZSM-5 catalysts (Si/Al ratio of 15 and 9) using diketene-acetone (2,2,6-trimethyl-4H-1,3-dioxin-4-one) as ketene precursor under atmospheric

Hydrogenation of arenes and N-heteroaromatic compounds over ruthenium nanoparticles on poly(4-vinylpyridine): A versatile catalyst operating by a substrate-dependent dual site mechanism

A nanostructured catalyst composed of Ru nanoparticles immobilized on poly(4-vinylpyridine) (PVPy) has been synthesized by NaBH4 reduction of RuCl3·3H2O in the presence of the polymer in methanol at room temperature. TEM measurements show well-dispersed Ru nanoparticles with an average diameter of 3.1 nm. Both powder XRD patterns and XPS data indicate that the Ru particles are predominantly in the zerovalent state. The new catalyst is efficient for the hydrogenation of a wide variety of aromatic hydrocarbons and N-heteroaromatic compounds representative of components of petroleum-derived fuels. The experimental data indicate the existence of two distinct active sites in the nanostructure that lead to two parallel hydrogenation pathways, one for simple aromatics involving conventional homolytic hydrogen splitting on Ru and a second one for N-heteroaromatics taking place via a novel heterolytic hydrogen activation on the catalyst surface, assisted by the basic pyridine groups of the support.

Fused cycloalkyl amides and acids and their therapeutic applications

The present invention relates to the use of compounds of formula (I) for the treatment of epilepsy, bipolar disorder, psychiatric disorders, migraine, pain, or movement disorders, and to provide neuroprotection.