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7418-16-8

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7418-16-8 Usage

General Description

2,2-BIS(4-OXOCYCLOHEXYL)PROPANE, also known as Ketonic resin CH-82, is a chemical compound often used as a raw material for thermosetting coatings and adhesives. It is a colorless to pale yellow liquid with a high boiling point, making it suitable for high temperature applications. 2,2-BIS(4-OXOCYCLOHEXYL)PROPANE is also known for its excellent heat and chemical resistance, as well as its low viscosity and good flow properties. Its unique structure and properties make it a valuable ingredient in the production of high-performance coatings and adhesives for various industries, including automotive, aerospace, and industrial manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 7418-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7418-16:
(6*7)+(5*4)+(4*1)+(3*8)+(2*1)+(1*6)=98
98 % 10 = 8
So 7418-16-8 is a valid CAS Registry Number.

7418-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-Bis(4-oxocyclohexyl)propane

1.2 Other means of identification

Product number -
Other names 4-[2-(4-oxocyclohexyl)propan-2-yl]cyclohexan-1-one

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:7418-16-8 SDS

7418-16-8Downstream Products

7418-16-8Relevant articles and documents

The cyclohexanone derivative

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Paragraph 0025-0026; 0029-0033, (2021/10/13)

[Problem] to the cyclohexanone derivative, which can be efficiently manufactured at a low cost in a safe method. One or more of the hydroxy groups in one or more of benzene and 1 2 [a] having 6 - 30 carbon atoms in the raw material compound, in the presence of a hydrogenation catalyst in a solvent by, one or more of cyclohexanone derivative comprises one or more ketone structure 1 has a structure in which cyclohexanone 2 method, cyclohexanone is used as a solvent containing an alcohol derivative. [Drawing] no

Process for producing alicyclic monoketones and process for producing alicyclic diketones

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, (2008/06/13)

The process for producing alicyclic monoketones (hydroxyphenylcyclohexanone derivatives) according to the present invention comprises hydrogenating substituted bisphenols such as bisphenol A in a solvent in the presence of a palladium/alkali metal catalyst in which palladium and an alkali metal are both supported on a carrier to obtain alicyclic monoketones such as 2-(4-oxocyclohexyl)-2-(4-hydroxyphenyl)propane. The process for producing alicyclic diketones according to the present invention comprises hydrogenating substituted bisphenols such as bisphenol A in a solvent in the presence of a palladium/alkali metal catalyst in which palladium and an alkali metal are both supported on a carrier to obtain alicyclic diketones such as 2,2-bis(4-oxocyclohexyl)propane and 4,4′-bicyclohexanone. The other process for producing alicyclic monoketones according to the present invention comprises hydrogenating biphenols such as bis(4-hydroxyphenyl) in an organic solvent in the presence of a palladium catalyst in which 10 to 30% by weight of palladium is supported on a carrier to obtain alicyclic monoketones such as 4(4′-hydroxyphenyl)cyclohexanone. According to the present invention, alicyclic monoketones or alicyclic diketones can be obtained with high selectivity and in high yields through simple steps, because the process includes only one reaction step to hydrogenate substituted bisphenols under relatively mild conditions.

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