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N-Ethyl-N,N'-diphenylthiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15093-51-3

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15093-51-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15093-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,9 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15093-51:
(7*1)+(6*5)+(5*0)+(4*9)+(3*3)+(2*5)+(1*1)=93
93 % 10 = 3
So 15093-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N2S/c1-2-17(14-11-7-4-8-12-14)15(18)16-13-9-5-3-6-10-13/h3-12H,2H2,1H3,(H,16,18)

15093-51-3SDS

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 N-Ethyl-N,N'-diphenylthiourea

1.2 Other means of identification

Product number -
Other names N-Aethyl-N,N'-diphenyl-thioharnstoff

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:15093-51-3 SDS

15093-51-3Relevant academic research and scientific papers

Photocatalytic synthesis of unsymmetrical thiourea derivativesviavisible-light irradiation using nitrogen-doped ZnO nanorods

Koohgard, Mehdi,Sarvestani, Abdollah Masoudi,Hosseini-Sarvari, Mona

supporting information, p. 14505 - 14512 (2020/09/21)

An efficient, mild, and environmentally friendly route has been developed for the synthesis of unsymmetrical thiourea derivatives in moderate yields by the reaction of tertiary aromatic and aliphatic amines with phenyl-iso-thiocyanate in the presence of N-ZnO as a photocatalyst under visible-light irradiation. This method provides a pathway to activate the tertiary aromatic and aliphatic aminesviaC-N bond cleavage.

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