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1759-64-4

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1759-64-4 Usage

General Description

1,6-Dimethylcyclohexene is a chemical compound classified as a cyclic hydrocarbon and an alkene. It is composed of a six-membered carbon ring with two methyl groups attached at the first and sixth carbon positions. 1,6-DIMETHYLCYCLOHEXENE is commonly used as an intermediate in the production of various chemicals, including fragrances, pharmaceuticals, and polymers. 1,6-Dimethylcyclohexene has the potential to undergo polymerization reactions and can be used as a monomer in the synthesis of polymers. It is also known for its use as a precursor in the preparation of other organic compounds through various chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1759-64-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1759-64:
(6*1)+(5*7)+(4*5)+(3*9)+(2*6)+(1*4)=104
104 % 10 = 4
So 1759-64-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-7-5-3-4-6-8(7)2/h5,8H,3-4,6H2,1-2H3

1759-64-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-DIMETHYLCYCLOHEXENE

1.2 Other means of identification

Product number -
Other names 1,6-Dimethyl-1-cyclohexene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1759-64-4 SDS

1759-64-4Relevant articles and documents

Siegel et al.

, p. 2802,2803, 2806 (1966)

Ionic-liquid-like copolymer stabilized nanocatalysts in ionic liquids: II. Rhodium-catalyzed hydrogenation of arenes

Zhao, Chen,Wang, Han-zhi,Yan, Ning,Xiao, Chao-xian,Mu, Xin-dong,Dyson, Paul J.,Kou, Yuan

, p. 33 - 40 (2008/09/18)

Rhodium nanoparticles stabilized by the ionic-liquid-like copolymer poly[(N-vinyl-2-pyrrolidone)-co-(1-vinyl-3-butylimidazolium chloride)] were used to catalyze the hydrogenation of benzene and other arenes in ILs. The nanoparticle catalysts can endure forcing conditions (75 °C, 40 bar H2), resulting in high reaction rates and high conversions compared with other nanoparticles that operate in ILs. The hydrogenation of benzene attained record total turnovers of 20,000, and the products were easily separated without being contaminated by the catalysts. Other substrates, including alkyl-substituted arenes, phenol, 4-n-propylphenol, 4-methoxylphenol, and phenyl-methanol, were studied and in most cases were found to afford partially hydrogenated products in addition to cyclohexanes. In-depth investigations on reaction optimization, including characterization of copolymers, transmission electron microscopy, and an infrared spectroscopic study of nanocatalysts, were also undertaken.

Catalytic hydrohydrazination of a wide range of alkenes with a simple Mn complex

Waser, Jerome,Carreira, Erick M.

, p. 4099 - 4102 (2007/10/03)

Enhanced activity, lower catalyst loading, shorter reaction times, and expanded substrate scope are the advantages of [Mn(dpm)3] over Co catalysts in the hydrohydrazination reaction of alkenes (see scheme). Thus, sterically hindered alkenes, including tetrasubstituted alkenes, can now also readily undergo this reaction.

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