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Phenol, 2,2'-[(cyclohexylimino)bis(methylene)]bis[4,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118980-75-9

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118980-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118980-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,8 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118980-75:
(8*1)+(7*1)+(6*8)+(5*9)+(4*8)+(3*0)+(2*7)+(1*5)=159
159 % 10 = 9
So 118980-75-9 is a valid CAS Registry Number.

118980-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[cyclohexyl-[(2-hydroxy-3,5-dimethylphenyl)methyl]amino]methyl]-4,6-dimethylphenol

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:118980-75-9 SDS

118980-75-9Relevant academic research and scientific papers

Lactide Lactone Chain Shuttling Copolymerization Mediated by an Aminobisphenolate Supported Aluminum Complex and Al(O iPr)3: Access to New Polylactide Based Block Copolymers

Bonnet, Fanny,Bria, Marc,Chirachanchai, Suwabun,Favrelle, Audrey,Meimoun, Julie,Roussel, Pascal,Stoclet, Grégory,Sutapin, Choltirosn,Zinck, Philippe

supporting information, p. 21206 - 21210 (2021/12/17)

The chain shuttling ring-opening copolymerization of l-lactide with ?-caprolactone has been achieved using two aluminum catalysts presenting different selectivities and benzyl alcohol as chain transfer agent. A newly synthesized aminobisphenolate supporte

Self termination of ring opening reaction of p-substituted phenol-based benzoxazines: An obstructive effect via intramolecular hydrogen bond

Chirachanchai, Suwabun,Laobuthee, Apirat,Phongtamrug, Suttinun

experimental part, p. 714 - 721 (2009/12/01)

(Chemical Equation Presented) The ring opening polymerizations of p-substituted phenol-based benzoxazines are self-terminated as soon as dimers form. The polymerization of benzoxazine monomers does not proceed according to the theoretical mechanism even though the conditions, temperature, molar ratio, solvent polarity, and reactant ratio are varied. The speculated mechanism, involving the unique structure of a dimer with interand intramolecular hydrogen bonds, is applied to explain an obstructive effect on ring opening polymerization. In this article, we clarify an important case which the stereo structure of the compound controls the reaction and prevents the polymerization expected from the theoretical mechanism.

Selective crown ether based macrocyclization: a model case study from N,N-bis(2-hydroxyalkylbenzyl)alkylamine

Chirachanchai, Suwabun,Rungsimanon, Thitiporn,Phongtamrug, Suttinun,Miyata, Mikiji,Laobuthee, Apirat

experimental part, p. 5855 - 5861 (2009/12/01)

A model case of selective crown ether based macrocycles, i.e., [1+1] or [2+2] macrocycles, obtained from a simple reaction of N,N-bis(2-hydroxyalkylbenzyl)alkylamine, HBA, and ditosylated compounds is proposed. For HBA with the methyl group at ortho and p

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