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[3,3'(4H,4'H)-Biquinazoline]-4,4'-dione, 1,2-dihydro-2-(4-methylphenyl)-2'-phenylis a chemical compound belonging to the biquinazoline class, characterized by the presence of two quinazoline rings. This specific compound features a 1,2-dihydro-2-(4-methylphenyl)-2'-phenylsubstituent, which highlights the attachment of a dihydroquinazoline ring with a 4-methylphenyl and phenyl group. Biquinazoline derivatives, including [3,3'(4H,4'H)-Biquinazoline]-4,4'-dione, 1,2-dihydro-2-(4-methylphenyl)-2'-phenyl-, have been investigated for their potential biological activities, such as anticancer and antimicrobial properties.

190514-74-0

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190514-74-0 Usage

Uses

Used in Pharmaceutical Industry:
[3,3'(4H,4'H)-Biquinazoline]-4,4'-dione, 1,2-dihydro-2-(4-methylphenyl)-2'-phenylis used as a potential therapeutic agent for its anticancer properties. [3,3'(4H,4'H)-Biquinazoline]-4,4'-dione,
1,2-dihydro-2-(4-methylphenyl)-2'-phenylhas been studied for its ability to target and inhibit the growth of cancer cells, making it a promising candidate for the development of novel cancer treatments.
Used in Antimicrobial Applications:
In the field of antimicrobial research, [3,3'(4H,4'H)-Biquinazoline]-4,4'-dione, 1,2-dihydro-2-(4-methylphenyl)-2'-phenylis utilized as a potential agent against various microorganisms. Its ability to inhibit microbial growth suggests that it could be a valuable component in the development of new antimicrobial drugs or treatments.
Used in Chemical Research:
This biquinazoline derivative is also used in chemical research as a model compound to study the structure-activity relationships of biquinazoline compounds. Understanding the properties and reactivity of [3,3'(4H,4'H)-Biquinazoline]-4,4'-dione, 1,2-dihydro-2-(4-methylphenyl)-2'-phenyl- can provide insights into the design and synthesis of new biquinazoline-based molecules with improved biological activities and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 190514-74-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,5,1 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190514-74:
(8*1)+(7*9)+(6*0)+(5*5)+(4*1)+(3*4)+(2*7)+(1*4)=130
130 % 10 = 0
So 190514-74-0 is a valid CAS Registry Number.

190514-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-[2-(4'-methylphenyl)-4-oxo-1,2,3,4-tetrahydroquinazolin-3-yl]quinazolin-4(3H)-one

1.2 Other means of identification

Product number -
Other names 2'-Phenyl-2-p-tolyl-1,2-dihydro-[3,3']biquinazolinyl-4,4'-dione

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:190514-74-0 SDS

190514-74-0Downstream Products

190514-74-0Relevant academic research and scientific papers

Bisazaheterocyclics: Part V - Synthesis of some quinazolinonyl/benzodiazepinonyl - quinazolinones

Reddy, G. Mahesh,Reddy, P. S. N.

, p. 689 - 693 (2007/10/03)

2-Phenyl-3-(2-aminobenzamido)quinazolin-4(3H)-one 1 reacts with aldehydes, phenylisocyanate and chloroacetyl chloride to give 2-phenyl-3-(2-alkyl/aryl-4-oxo-1,2,3,4-tetrahydroquinazolin-3-yl)quinazolin-4(3H)-ones 2, 2-phenyl-3-(2,4-dioxo-1,2,3,4-tetrahydr

2-Phenyl-3-(2-aminobenzamido)quinazolin-4(3H)-one as a synthon for bisazaheterocvclics

Reddy, G. Mahesh,Reddy, P. S. N.

, p. 166 - 168 (2007/10/03)

Synthesis of 2-phenyl-3-(2-aminobenzamido)quinazolin-4(3H)-one 7, a synthon of unsymmetrical bisazaheterocyclics, is reported from 3-amino-2-phenylquinazolin-4(3H)-one 2. In an alternate synthetic route 7 has been prepared by refluxing 2-aminobenzoylhydrazine and 2-phenyl-3,1-benzoxazin-4(H)-one 1 in pyridine.

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