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4(3H)-Quinazolinone, 3-[[(4-hydroxy-3-methoxyphenyl)methylene]amino]-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106873-10-3

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106873-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106873-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,7 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106873-10:
(8*1)+(7*0)+(6*6)+(5*8)+(4*7)+(3*3)+(2*1)+(1*0)=123
123 % 10 = 3
So 106873-10-3 is a valid CAS Registry Number.

106873-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-{[(4-hydroxy-3-methoxyphenyl)methylene]amino}-2-phenylquinazolin-4(3H)-one

1.2 Other means of identification

Product number -
Other names 2-phenyl-3-amino-4(3H)-quinazolone-vanillin

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:106873-10-3 SDS

106873-10-3Relevant academic research and scientific papers

Synthesis, spectroscopic characterization, antineoplastic, in vitro-cytotoxic, and antibacterial activities of mononuclear ruthenium(II) complexes

Thota, Sreekanth,Imran, Mohammad,Udugula, Manasa,Karki, Subhas Somalingappa,Kanjarla, Narasimha,Yerra, Rajeshwar,Balzarini, Jan,De Clercq, Erik

, p. 823 - 839 (2012)

The synthesis, antineoplastic, cytotoxic, and antibacterial activities of Ru(II) complexes derived from quinazoline and thiosemicarbazone ligands are reported. These complexes have been prepared and characterized by UV-Vis, IR, 1H-NMR, FAB-mass

Antibacterial activity of some 3-(arylideneamino)-2-phenylquinazoline-4(3H) -ones: Synthesis and preliminary QSAR studies

Nanda, Ashis Kumar,Ganguli, Subarna,Chakraborty, Ranadhir

, p. 2413 - 2426 (2008/03/11)

Synthesis of ten 3-(arylideneamino)-2-phenylquinazoline-4(3H)-ones is reported. All the compounds contained a common phenyl group at the 2-position, while the substituents on the arylideneamino group were varied. The compounds were investigated for their

Synthesis and Biological Activities of 3-(2'-Aryl-4'-oxothiazolidin-3'-yl)-2-phenylquinazolin-4(3H)-ones

Husain, M. I.,Shukla, Sarveshwar

, p. 545 - 548 (2007/10/02)

A number of 3-(2'-aryl-4'-oxothiazolidin-3'-yl)-2-phenyl-quinazolin-4(3H)-ones (III) have been synthesised and screened for their possible antibacterial activity and CNS activity on albino mice.Some chemical leads towards structure-activity relationship h

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