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Methanone, bis(2,3,5,6-tetramethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67075-68-7

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67075-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67075-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67075-68:
(7*6)+(6*7)+(5*0)+(4*7)+(3*5)+(2*6)+(1*8)=147
147 % 10 = 7
So 67075-68-7 is a valid CAS Registry Number.

67075-68-7SDS

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 bis(2,3,5,6-tetramethylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2,2',3,3',5,5',6,6'-Octamethyl-benzophenon

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:67075-68-7 SDS

67075-68-7Relevant academic research and scientific papers

Ultrafast Chemistry: Cobalt Carbonyl-Mediated Synthesis of Diaryl Ketones under Microwave Irradiation

Enquist, Per-Anders,Nilsson, Peter,Larhed, Mats

, p. 4875 - 4878 (2007/10/03)

(Equation Presented) By combining the advantages of metal activation, in situ carbon monoxide delivery, and microwave heating, benzophenones were efficiently synthesized in 6-10 s. These ultrafast carbonylation reactions occur under air by flash heating o

Polymethylated and poly(tert)butylated diphenylcarbenes. Generation, reactions, kinetics, and deuterium isotope effects of sterically congested triplet carbenes

Tomioka, Hideo,Okada, Hidetsumu,Watanabe, Tetsuya,Banno, Kohji,Komatsu, Kazunori,Hirai, Katsuyuki

, p. 1582 - 1593 (2007/10/03)

Dimesitylcarbene (2a) was shown to decay by undergoing dimerization and to have a half-life of 160 ms, some 5 orders of magnitude longer-lived than diphenylcarbene. Didurylcarbene (2b) was twice as long-lived as 2a, while decamethyldiphenylcarbene (2c) de

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