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1-(o-Tolyl)quinazolin-4(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90071-27-5

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90071-27-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

Quinazolinone is a class of compounds that have a quinazoline ring fused with a ketone group. 1-(o-Tolyl)quinazolin-4(1H)-one belongs to this class.

Explanation

The compound is used in the pharmaceutical industry due to its potential therapeutic properties, which include anti-inflammatory, anti-cancer, and anti-tumor activities.
4. Anti-inflammatory Activity

Explanation

1-(o-Tolyl)quinazolin-4(1H)-one has been studied for its ability to reduce inflammation, which can be beneficial in treating various inflammatory diseases.
5. Anti-cancer Activity

Explanation

The compound has shown potential in inhibiting the growth of cancer cells, making it a candidate for further research in cancer treatment.
6. Anti-tumor Activity

Explanation

1-(o-Tolyl)quinazolin-4(1H)-one has been investigated for its ability to inhibit tumor growth, which could be useful in the development of new cancer treatments.
7. Enzyme Inhibition

Explanation

The compound acts as an inhibitor of certain enzymes, which can be crucial in disrupting the biochemical pathways involved in disease progression.

Explanation

Preclinical studies, which are conducted before testing the compound on humans, have shown promising results for the potential use of 1-(o-Tolyl)quinazolin-4(1H)-one in treating various diseases.

Explanation

The compound has been explored for its potential use in the development of new drugs and pharmaceutical products, due to its various therapeutic properties and enzyme inhibition capabilities.

Class

Quinazolinone

Pharmaceutical Industry

Potential therapeutic properties

Preclinical Studies

Promising results

Drug Development

Potential use in new drugs and pharmaceutical products

Check Digit Verification of cas no

The CAS Registry Mumber 90071-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90071-27:
(7*9)+(6*0)+(5*0)+(4*7)+(3*1)+(2*2)+(1*7)=105
105 % 10 = 5
So 90071-27-5 is a valid CAS Registry Number.

90071-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylphenyl)quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 1-o-Toluyl-1,4-dihydrochinazolin-4-on

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:90071-27-5 SDS

90071-27-5Relevant academic research and scientific papers

Composes Sulfures Heterocycliques. CII. Action de l'hydroxylamine sur les dihydro-1,2 benzothiazine-3,1 thiones-4

Legrand, Louis,Lozac'h, Noel

, p. 1615 - 1623 (2007/10/02)

Hydroxylamine reacts with 1-alkyl-1,2-dihydro-3,1-benzothiazine-4-thiones (1), giving 1-alkyl-3-hydroxy-2,3-dihydro-1H-quinazoline-4-thiones (2).The same reagent, in neutral medium, converts 1-aryl-1,2-dihydro-3,1-benzothiazine-4-thiones (3) into 1-aryl-4

Composes Sulfures Heterocycliques. C. Action de la methylhydrazine et de la N,N-dimethylhydrazine sur les dihydro-1,2 benzothiazine-3,1 thiones-4

Legrand, Louis,Lozac'H, Noel

, p. 217 - 225 (2007/10/02)

Methylhydrazine or N,N-dimethylhydrazine react with various 1,2-dihydro-3,1-benzothiazine-4-thiones substituted, in position 1, either by an alkyl (1) or an aryl (5).Alkyl derivatives 1 lead to 1-alkyl-3-methylamino (or 3-dimethylamino)-2,3-dihydro-1H-qui

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