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Thiourea, N-(3-methylphenyl)-N'-phenyl-, also known as 3-methyl-N-phenyl-N'-phenylthiourea or 3-Methyl-N,N'-diphenylthiourea, is an organic compound with the chemical formula C15H14N2S. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. Thiourea, N-(3-methylphenyl)-N'-phenyl- is primarily used as an analytical reagent for the detection of certain metal ions, particularly copper, silver, and mercury, due to its ability to form colored complexes with these ions. It is also employed in the synthesis of various organic compounds and as a building block in the preparation of pharmaceuticals and dyes. The compound is characterized by its unique structure, which includes a thiourea core with two phenyl groups and a methyl group attached to one of the phenyl rings, contributing to its chemical properties and reactivity.

1215-91-4

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1215-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1215-91:
(6*1)+(5*2)+(4*1)+(3*5)+(2*9)+(1*1)=54
54 % 10 = 4
So 1215-91-4 is a valid CAS Registry Number.

1215-91-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methylphenyl)-3-phenylthiourea

1.2 Other means of identification

Product number -
Other names Thiourea,N-(3-methylphenyl)-N'-phenyl

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:1215-91-4 SDS

1215-91-4Relevant academic research and scientific papers

Hydroamination and Hydrophosphination of Isocyanates/Isothiocyanates under Catalyst-Free Conditions

Zhu, Xiancui,Xu, Mengchen,Sun, Jinrong,Guo, Dianjun,Zhang, Yiwei,Zhou, Shuangliu,Wang, Shaowu

, p. 5213 - 5218 (2021/10/19)

Symmetrical and unsymmetrical N,N’-disubstituted as well as trisubstituted ureas/thioureas by the hydroamination of isocyanates/isothiocyanates, and various phosphathioureas by the hydrophosphination of isothiocyanates have been synthesized in good to excellent yields under catalyst-free and mild conditions. This protocol is also applicable for the efficient synthesis of chiral ureas and thioureas and common herbicides, such as fenuron and monuron.

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