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100558-60-9

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100558-60-9 Usage

General Description

(4-ethylcyclohexyl)benzene is a chemical compound with the molecular formula C14H20. It is an aromatic hydrocarbon with a benzene ring and a cyclohexyl group, and an ethyl substituent at the fourth carbon atom of the cyclohexyl ring. (4-ethylcyclohexyl)benzene is commonly used as a precursor in the production of various polymers and resins, and it also serves as a starting material for the synthesis of other organic compounds. It is known for its low toxicity and is considered to be relatively stable under normal conditions. Additionally, (4-ethylcyclohexyl)benzene has been studied for its potential applications in the fields of pharmaceuticals, fragrances, and flavoring agents.

Check Digit Verification of cas no

The CAS Registry Mumber 100558-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,5 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100558-60:
(8*1)+(7*0)+(6*0)+(5*5)+(4*5)+(3*8)+(2*6)+(1*0)=89
89 % 10 = 9
So 100558-60-9 is a valid CAS Registry Number.

100558-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-ethylcyclohexyl)benzene

1.2 Other means of identification

Product number -
Other names trans-1-Ethyl-4-phenylcyclohexan

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:100558-60-9 SDS

100558-60-9Downstream Products

100558-60-9Relevant articles and documents

Aliphatic Liquid Crystals, 9. - Stereospecific Reduction of 1-Acyl- to 1-Alkyl-4-phenylcyclohexanes

Sucrow, Wolfgang,Heider, RRoland,Joraschek, Norbert

, p. 1039 - 1044 (2007/10/02)

The title reaction - important for the synthesis of aliphatic liquid crystals - is accomplished by reduction of the tosylhydrazones with sodium cyanoborohydride.While the trans-configurated model ketones 6a, 7a give the tosylhydrazones 10a, 11a, and these

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