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

105886-56-4

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105886-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105886-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105886-56:
(8*1)+(7*0)+(6*5)+(5*8)+(4*8)+(3*6)+(2*5)+(1*6)=144
144 % 10 = 4
So 105886-56-4 is a valid CAS Registry Number.

105886-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methyl-4-oxoquinazolin-3-yl)-3-(3-methylphenyl)thiourea

1.2 Other means of identification

Product number -
Other names -

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:105886-56-4 SDS

105886-56-4Relevant 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.

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 of substituted quinazolone derivatives as potential anti-HIV agents (part III)

Desai,Bhatt,Shah,Undavia,Trivedi,Narayanan

, p. 361 - 366 (2007/10/03)

Several 1-[2-phenyl-4(4H)-oxo-3-quinazolinyl]-2-methyl-4-arylidine -5-oxo-imidazolines (Va-1), 2-phenyl-3-(aroyl amino)-4(4H)-oxo quinazolines (Vla-I) and N1-2-methyl-4(4H)-oxo-3-quinazolinyl-N2-aryl-thioureas (Vlla-k), have been synthesised and tested for anti-HIV activity. The structures of these compounds have been established on the basis of elemental analysis and spectral data.

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