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Trisiloxane, 3-cyclohexyl-1,1,1,3,5,5,5-heptamethyl-, also known as 3-cyclohexyl-1,1,1,3,5,5,5-heptamethyltrisiloxane, is a cyclic siloxane compound with the molecular formula C13H28Si3O3. It consists of a cyclohexyl group attached to a trisiloxane chain, which is composed of three silicon atoms connected by oxygen atoms. This chemical is primarily used as a component in various industrial applications, such as lubricants, surfactants, and as a coupling agent in the production of silicone-based materials. Due to its unique structure and properties, it offers excellent thermal stability, low toxicity, and high chemical resistance, making it a valuable compound in the chemical industry.

14579-59-0

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14579-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14579-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,7 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14579-59:
(7*1)+(6*4)+(5*5)+(4*7)+(3*9)+(2*5)+(1*9)=130
130 % 10 = 0
So 14579-59-0 is a valid CAS Registry Number.

14579-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl-methyl-bis(trimethylsilyloxy)silane

1.2 Other means of identification

Product number -
Other names Trisiloxane,3-cyclohexyl-1,1,1,3,5,5,5-heptamethyl

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:14579-59-0 SDS

14579-59-0Downstream Products

14579-59-0Relevant academic research and scientific papers

INTERMOLECULAR C-H SILYLATION OF UNACTIVATED ARENES

-

Paragraph 00131, (2015/03/28)

Reaction mixtures for silvlating arene substrates and methods of using such reaction mixtures to silyiate the arene substrates are provided. Exemplary reaction mixtures include the arene substrate, a liganded metal catalyst, a hydrogen acceptor and an organic solvent. The reaction conditions allow for diverse substituents on the arene substrate.

Mechanism of the rhodium-catalyzed silylation of arene C-H bonds

Cheng, Chen,Hartwig, John F.

supporting information, p. 12064 - 12072 (2014/10/16)

Mechanistic studies on the rhodium-catalyzed silylation of arene C-H bonds are reported. The resting state of the catalyst was fully characterized by NMR spectroscopy and X-ray diffraction and was determined to be a phosphine-ligated Rh(III) silyl dihydri

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