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N-(2-benzoylphenyl)thiophene-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41296-65-5

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41296-65-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41296-65-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,9 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41296-65:
(7*4)+(6*1)+(5*2)+(4*9)+(3*6)+(2*6)+(1*5)=115
115 % 10 = 5
So 41296-65-5 is a valid CAS Registry Number.

41296-65-5SDS

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 Thiophene-2-carboxylic acid (2-benzoyl-phenyl)-amide

1.2 Other means of identification

Product number -
Other names α-THENOYLAMIDO-2 BENZOPHENONE

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:41296-65-5 SDS

41296-65-5Relevant academic research and scientific papers

Titanium-Induced Syntheses of Furans, Benzofurans and Indoles

Fuerstner, Alois,Jumbam, Denis N.

, p. 5991 - 6010 (2007/10/02)

Highly reactive titanium on graphite as the reagent of choice promotes intramolecular McMurry type reactions of acyloxy- and acylamido carbonyl compounds affording furans, benzofurans and indoles in good to excellent yields.A variety of reducible groups in the substrates is tolerated (e.g. -F, -Cl, -Br, -I, -CF3, -OMe, -CN, -thiophenyl, -COOR, -CONR2) and strained products such as 11h can be obtained, the X-ray analysis of which is reported.The experimental results indicate the possible formation of dianions from the aromatic aldehydes or ketones as reactive intermediates which attack the ester or amide functions in their proximity, rather than a radical path via ketyls.

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