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Phenol, 2,6-dipentyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116374-97-1

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116374-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116374-97-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,7 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116374-97:
(8*1)+(7*1)+(6*6)+(5*3)+(4*7)+(3*4)+(2*9)+(1*7)=131
131 % 10 = 1
So 116374-97-1 is a valid CAS Registry Number.

116374-97-1SDS

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 2,6-dipentylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2,6-dipentyl

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:116374-97-1 SDS

116374-97-1Relevant academic research and scientific papers

Synthesis of 4-(3,5-dialkyl-4-hydroxyphenyl)pyridines

Combellas,Suba,Thiebault

, p. 4923 - 4926 (2007/10/02)

Starting from 4-chloropyridine and 2,6-dialkylphenoxides, 4-(3,5-dialkyl-4-hydroxyphenyl)pyridines are obtained via an electrochemical induced S(RN)1 reaction using 2,4'-bipyridine as a mediator (alkyl = pentyl, isopropyl, methyl). Quaternization of 4-(3,

Facile Synthesis of 2,6-Dialkylphenols by Cross-Aromatization of Cyclohexanones with Aldehydes Catalyzed by Zirconocene Complexes

Nakano, Tatsuya,Shirai, Hideki,Tamagawa, Hiroshi,Ishii, Yasutaka,Ogawa, Masaya

, p. 5181 - 5183 (2007/10/02)

2,6-Dialkylphenols, which are difficult to prepare by conventional methods, have been conveniently synthesized in one step via zirconocene-catalyzed cross-aromatization of cyclohexanones with aldehydes.

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