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N-[(phenylcarbonothioyl)carbamoyl]benzamide is a complex organic compound with the chemical formula C14H12N2O2S. It is a derivative of benzamide, featuring a phenylcarbonothioyl group attached to the carbamoyl moiety. N-[(phenylcarbonothioyl)carbamoyl]benzamide is characterized by its aromatic structure, with a benzene ring connected to a carbonothioyl group (a carbonyl group bonded to a sulfur atom), which in turn is linked to another benzene ring through a carbamoyl group (a carbonyl group bonded to an amine). The compound may have potential applications in pharmaceuticals or as a chemical intermediate due to its unique structure and reactivity. However, specific uses and properties would require further investigation and research.

3553-70-6

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3553-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3553-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3553-70:
(6*3)+(5*5)+(4*5)+(3*3)+(2*7)+(1*0)=86
86 % 10 = 6
So 3553-70-6 is a valid CAS Registry Number.

3553-70-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(benzenecarbonothioylcarbamoyl)benzamide

1.2 Other means of identification

Product number -
Other names 1-Benzoyl-3-thiobenzoyl-harnstoff

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:3553-70-6 SDS

3553-70-6Downstream Products

3553-70-6Relevant academic research and scientific papers

Thioacyl Isocyanates, XV. Reaction with Nucleophilic C-Compounds

Goerdeler, Joachim,Tiedt, Marie-Louise,Nandi, Kumaresh

, p. 2713 - 2722 (2007/10/02)

Reaction of thioacyl isocyanates with sodium ethylmalonate and related compounds affords 1, existing as amides or tautomers; they are suitable as starting material for the synthesis of 2, 3, 4. - Thiobenzoyl isocyanate reacts with nucleophilic alkenes and

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