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Cyclohexane, 1,2,3,4,5,6-hexamethyl-, also known as hexamethylcyclohexane, is an organic compound with the chemical formula C12H24. It is a derivative of cyclohexane, where six methyl groups (CH3) are attached to each of the six carbon atoms in the cyclohexane ring. Cyclohexane, 1,2,3,4,5,6-hexamethyl- is a colorless, flammable liquid with a low melting point and boiling point, and it is insoluble in water. Hexamethylcyclohexane is used as a solvent, a chemical intermediate, and a component in various industrial applications, such as the production of lubricants, rubber, and plastics. It is also known for its low toxicity and high thermal stability, making it a preferred choice in certain chemical processes.

1795-13-7

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1795-13-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1795-13-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1795-13:
(6*1)+(5*7)+(4*9)+(3*5)+(2*1)+(1*3)=97
97 % 10 = 7
So 1795-13-7 is a valid CAS Registry Number.

1795-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5,6-hexamethylcyclohexane

1.2 Other means of identification

Product number -
Other names 1r,2c,3c,4c,5c,6c-Hexamethylcyclohexan

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:1795-13-7 SDS

1795-13-7Downstream Products

1795-13-7Relevant academic research and scientific papers

A novel reduction of polycarboxylic acids into their corresponding alkanes using n-butylsilane or diethylsilane as the reducing agent

Nimmagadda, Rama D.,McRae, Christopher

, p. 3505 - 3508 (2007/10/03)

A convenient one-pot reaction has been developed for the reduction of polycarboxylic acids on aliphatic and aromatic systems to their corresponding alkanes. The reduction utilises either diethylsilane or n-butylsilane as the reducing agent in the presence of the Lewis acid catalyst tris(pentafluorophenyl)borane.

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