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Thiourea, N-(4-chlorophenyl)-N'-(2-hydroxyethyl)-, also known as 4-chlorophenylthiourea or 4-chlorophenyl-N-(2-hydroxyethyl)thiourea, is an organic compound with the chemical formula C8H9ClN2OS. It is a derivative of thiourea, featuring a 4-chlorophenyl group attached to one nitrogen atom and a 2-hydroxyethyl group attached to the other nitrogen atom. Thiourea, N-(4-chlorophenyl)-N'-(2-hydroxyethyl)- is a white crystalline solid and is soluble in water and ethanol. It has various applications in the chemical industry, such as a reagent in organic synthesis and a building block for the production of pharmaceuticals and agrochemicals. Due to its potential reactivity and the presence of a chlorinated aromatic group, it is important to handle Thiourea, N-(4-chlorophenyl)-N'-(2-hydroxyethyl)- with care, following proper safety protocols.

1848-62-0

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1848-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1848-62-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 8 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1848-62:
(6*1)+(5*8)+(4*4)+(3*8)+(2*6)+(1*2)=100
100 % 10 = 0
So 1848-62-0 is a valid CAS Registry Number.

1848-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chloro-phenyl)-3-(2-hydroxy-ethyl)-thiourea

1.2 Other means of identification

Product number -
Other names 1-(p-Chlor-phenyl)-3-(2-hydroxy-ethyl)-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:1848-62-0 SDS

1848-62-0Relevant academic research and scientific papers

Synthesis of thiazol, thiazinan, thiadiazin, thiazolidin, triazine, thioxo-pyrimidin and thioxo-imidazolidine by inter-intra molecular cyclization

Zade, Mangesh N.,Katiya, Manish M.,Deotale, Vinod D.,Sontakke, Madhuri M.,Dhonde, Madhukar G.,Berad, Baliram N.

, p. 1493 - 1500 (2019/05/21)

Syntheses of five and six membered heterocyclic derivatives by the reaction of disubstituted thiocarbamides with interintramolecular cyclizations in catalyst free condition have been reported. The simple product isolation without column, good yields under mild condition, and applicable green matrix are the advantages of present protocol.

Synthesis and biological activity of novel symmetrical bis-2- phenyliminothiazolidine derivatives

Li, Gang-Yue,Qian, Xu-Hong,Yan, Sheng-Gang,Cui, Jing-Nan,Huang, Qing-Chun,Zhang, Rong,Liu, Feng-Yu,Cui, Da-Wei

, p. 2851 - 2861 (2007/10/03)

A series of novel symmetrical bis-2-phenyliminothiazolidine derivatives were designed and synthesized. The structures of all the title compounds were characterized by 1H NMR and, in some cases, by 13C NMR, IR, and high-resolution mas

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

Caujolle, Raymond,Amarouch, Hamid,Payard, Marc,Loiseau, Philippe R.,Bories, Christian,et al.

, p. 287 - 292 (2007/10/02)

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.

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