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Thiourea, N-(4-chlorophenyl)-N'-(2-methyl-4-oxo-3(4H)-quinazolinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96859-49-3

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96859-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96859-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,5 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96859-49:
(7*9)+(6*6)+(5*8)+(4*5)+(3*9)+(2*4)+(1*9)=203
203 % 10 = 3
So 96859-49-3 is a valid CAS Registry Number.

96859-49-3SDS

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 1-(4-chlorophenyl)-3-(2-methyl-4-oxoquinazolin-3-yl)thiourea

1.2 Other means of identification

Product number -
Other names N-(4-chlorophenyl)-N'-<2-methyl-4(3H)-quinazolinon-3-yl> thiourea

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:96859-49-3 SDS

96859-49-3Relevant academic research and scientific papers

Synthesis of some 2-methyl-3-(arylthiocarbamido) quinazol-4-ones and 2-methyl-3-(arylidencarboxamido) quinazol-4-ones as potential antimicrobial agents

Gupta

experimental part, p. 124 - 127 (2010/10/21)

Some quinazolone derivatives of 2-methyl-3-(arylthiocarbamido) quinazol-4-ones (2) and 2-methyl-3(arylidencarboxamido) quinazol-4-ones (3) have been synthesized and assayed for their possible antibacterial activity against Bacillus subtilis, Bacillus cereus, Salmonella aureus, Salmonella lutae and antiviral activity against Gomphrena mosaic virus. Some of these compounds show notable activity.

Synthesis, analgesic, anti-inflammatory and antibacterial activities of some novel 2-methyl-3-substituted quinazolin-4-(3H)-ones

Alagarsamy, Veerachamy,Murugananthan, Gopal,Venkateshperumal, Ramachandran

, p. 1711 - 1714 (2007/10/03)

A series of novel 2-methyl-3-substituted quinazolin-4-(3H)-ones have been synthesized by treating (2-methyl-4-oxo-3H-quinazolin-3-yl)dithiocarbamic acid methyl ester with different amines, the starting material dithiocarbamate was synthesized from anthranilic acid. The compounds synthesized were investigated for analgesic, anti-inflammatory and antibacterial activities. All the test compounds exhibited significant activity, the compounds VA2, VA3 and VA4 shown more potent analgesic activity, and the compounds VA3 and VA4 shown more potent anti-inflammatory activity than the reference compound diclofinac sodium.

Pharmacological studies of some 2-methyl-3-(arylthio-carbamido) quinazol-4-ones and 2-methyl-3-(aryliden-carboxamido) quinazol-4-ones

Srivastava, Manoj Kr.,Mishra, Bharati,Nizamuddin

, p. 342 - 344 (2007/10/03)

Some quinazolone derivatives of 2-methyl-3-(arylthio-carbamido)quinazol-4-ones 2 and 2-methyl-3-(aryliden-carboxamido) quinazol-4-ones 3 have been synthesised and assayed for their possible antibacterial activity against Bacillus subtilis, Bacillus cereus, Solmonella aureus, Solmonella lutae and antiviral activity against Gomphrena mosaic virus. Some of these compounds show notable activity.

Synthesis and anticonvulsant properties of some novel quinazolinone thiazolidine and 4-thiazolidone derivatives

El-Feky

, p. 894 - 896 (2007/10/02)

A series of quinazolinone thiazolidine and 4-thiazolidone derivatives were prepared. The structure of the isolated products have been confirmed by elemental analyses, spectroscopic data and ambiguous synthesis in certain cases. Some of these compounds wer

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