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N-(2-chloro-phenyl)-N'-(4-fluoro-phenyl)-thiourea is an organic compound with the molecular formula C13H9ClFN2S. It is a derivative of thiourea, featuring a thiourea functional group (-NH-CS-NH-) and two substituted phenyl rings. The 2-chloro-phenyl group is attached to the nitrogen atom at one end of the thiourea, while the 4-fluoro-phenyl group is attached to the nitrogen atom at the other end. N-(2-chloro-phenyl)-N'-(4-fluoro-phenyl)-thiourea is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science. It is characterized by its unique combination of halogenated aromatic rings, which can influence its chemical reactivity and physical properties.

368-07-0

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368-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 368-07-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 368-07:
(5*3)+(4*6)+(3*8)+(2*0)+(1*7)=70
70 % 10 = 0
So 368-07-0 is a valid CAS Registry Number.

368-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-chloro-phenyl)-N'-(4-fluoro-phenyl)-thiourea

1.2 Other means of identification

Product number -
Other names N-(2-Chlor-phenyl)-N'-(4-fluor-phenyl)-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:368-07-0 SDS

368-07-0Relevant academic research and scientific papers

An "on-water" exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles

Rout, Saroj Kumar,Guin, Srimanta,Nath, Jayashree,Patel, Bhisma K.

, p. 2491 - 2498 (2013/02/21)

An "on-water" one-pot process has been engineered for the preparation of 2-aminobenzothiazole from ortho-halo (-F, -Cl, -Br and -I) substituted unsymmetrical thioureas. For ortho -I and -Br substrates the reactions afford 2-aminobenzothiazoles under metal free condition promoted by base. However, the relatively inert ortho -Cl and -F substrates undergo intramolecular arylthiolation only in the presence of CuO nanoparticles yielding 2-aminobenzothiazoles. This methodology provides easy access to aminobenzothiazoles utilising even the ortho -Cl and -F substrates. The catalyst is recyclable several times without loss of substantial activity. Other remarkable features include the wide range of functional group tolerance, absence of chromatographic purification (for ortho -I and -Br substrates) and providing moderate to excellent yield of the products under mild conditions, thus rendering the methodology as a highly eco-friendly alternative to the existing methods.

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