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Ethanone, 1-(4-bromophenyl)-2-(3,4-dimethyl-2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

393085-12-6

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393085-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 393085-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,3,0,8 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 393085-12:
(8*3)+(7*9)+(6*3)+(5*0)+(4*8)+(3*5)+(2*1)+(1*2)=156
156 % 10 = 6
So 393085-12-6 is a valid CAS Registry Number.

393085-12-6SDS

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-(4-Bromophenacyl)-3,4-dimethylthiophene

1.2 Other means of identification

Product number -
Other names 1-(4-Bromo-phenyl)-2-(3,4-dimethyl-thiophen-2-yl)-ethanone

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:393085-12-6 SDS

393085-12-6Relevant academic research and scientific papers

Synthesis and thermal transformation of stable monocyclic λ4-thiabenzenes

Shimizu,Kudo,Kataoka,Hori

, p. 2269 - 2276 (2007/10/03)

The stable monocyclic λ4-thiabenzenes 6a-e, which are stabilized with electron-withdrawing substituents such as benzoyl, cyano and alkoxycarbonyl groups, are synthesized in high yields by proton abstraction from the corresponding thiopyranium salts 5a-e with triethylamine in ethanol. The ylidic properties of the λ4-thiabenzenes are established based on spectral and chemical evidence. Thermal decomposition of the λ4-thiabenzenes affords alkyl-rearranged products 7,8, and 9, thienofuran derivatives 10 (from benzoyl-substituted λ4-thiabenzenes), and thiophene derivatives 11. A plausible mechanism for the formation of those products is also discussed.

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