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Phenol, 4,4'-cyclohexylidenebis[2-chloro-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73008-80-7

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73008-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73008-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,0 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73008-80:
(7*7)+(6*3)+(5*0)+(4*0)+(3*8)+(2*8)+(1*0)=107
107 % 10 = 7
So 73008-80-7 is a valid CAS Registry Number.

73008-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-[1-(3-chloro-4-hydroxy-5-methylphenyl)cyclohexyl]-6-methylphenol

1.2 Other means of identification

Product number -
Other names 6,6'-dichloro-4,4'-cyclohexylidenedi-o-cresol

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:73008-80-7 SDS

73008-80-7Downstream Products

73008-80-7Relevant academic research and scientific papers

Synthesis and spectral study of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids with antimicrobial activity

Bhadja,Parsania

, p. 1699 - 1704 (2012/06/15)

Synthesis of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids (R,R′=H,CH3and Cl) by dissolving 0.1 mole bisphenols in 0.4 mole sodim hydroxide with drop wise addition of 0.2 mole chloroacetic acid. The reaction mixture refluxed for 4h at 60°C. Phenoxy acids have been confirmed by IR and NMR spectral characterization. The acids are also characterized by their antimicrobial and antifungal activities. The activities have been interpreted in light of bisphenol structures and the nature of substituent(s). The wide scale uses of bisphenol bioactive agents have brought many advantages to the agricultural industries.

Halogenated bisphenol-Z and derivatives thereof

-

, (2008/06/13)

Resistance to high heat distortion is imparted to high molecular weight aromatic polycarbonate resins by controlling the degree to which particular diphenols are halogenated so that there are obtained either highly pure dihalogenated diphenols or predeter

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