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[1,1'-Biphenyl]-2-ol, 3-cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20776-08-3

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20776-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20776-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,7 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20776-08:
(7*2)+(6*0)+(5*7)+(4*7)+(3*6)+(2*0)+(1*8)=103
103 % 10 = 3
So 20776-08-3 is a valid CAS Registry Number.

20776-08-3SDS

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-cyclohexyl-6-phenylphenol

1.2 Other means of identification

Product number -
Other names -

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:20776-08-3 SDS

20776-08-3Downstream Products

20776-08-3Relevant academic research and scientific papers

METHOD FOR THE PRODUCTION OF 4,4'-[1-TRIFLUOROMETHYL)ALKYLIDENE]-BIS-(2,6-DIPHENYLPHENOLS)

-

Page/Page column 10, (2010/12/29)

The present invention relates to a process for preparing 4,4′-[1-(trifluoromethyl)alkylidene]bis(2,6-diphenylphenols), in particular for preparing 4,4′-[1-(trifluoromethyl)ethylidene]bis(2,6-diphenylphenol), which comprises the self-condensation of cyclohexanone in the presence of a basic catalyst to form tricyclic condensation products, dehydrogenation of the resulting tricyclic condensation products in the presence of a supported transition metal catalyst in the condensed phase to form 2,6-diphenylphenol and reaction of the 2,6-diphenylphenol with a trifluoromethyl ketone. The invention further provides an improved process for preparing 2,6-diphenylphenol by aldol self-condensation of cyclohexanone.

Intramolecular Arene Hydrogenation at Niobium Metal Centres: Stereochemical Consequences

Steffey, Bryan D.,Rothwell, Ian P.

, p. 213 - 215 (2007/10/02)

Selective hydrogenation of 2,6-diphenylphenoxide to 2,6-dicyclohexylphenoxide ligands takes place at niobium(v) metal centres.

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