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1,2-dihydro-9H-pyrazolo[3,4-f]quinazolin-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73907-90-1

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73907-90-1 Usage

Type of compound

Heterocyclic compound

Elements present

Carbon (C), Hydrogen (H), Nitrogen (N), and Oxygen (O)

Structure

Contains both nitrogen and oxygen atoms

Derivation

Derived from pyrazolo[3,4-f]quinazolin-9-one

Usage

Used as a building block in the synthesis of various organic compounds

Potential applications

Medicinal chemistry and drug development

Importance

Its synthesis and characterization are crucial for understanding its potential uses and applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 73907-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73907-90:
(7*7)+(6*3)+(5*9)+(4*0)+(3*7)+(2*9)+(1*0)=151
151 % 10 = 1
So 73907-90-1 is a valid CAS Registry Number.

73907-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dihydropyrazolo[3,4-f]quinazolin-9-one

1.2 Other means of identification

Product number -
Other names 1-pyrazolo<3,4-f>quinazolin-9-(8H)-one

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:73907-90-1 SDS

73907-90-1Downstream Products

73907-90-1Relevant academic research and scientific papers

SYNTHESIS OF A -LINKED PYRAZOLOQUINAZOLINONE

Lichtenthaler, Frieder W.,Cuny, Eckehard

, p. 1053 - 1059 (2007/10/02)

A convenient synthesis is described for pyrazoloquinazolin-9-one (4), an internally expanded benzolog of the biologically relevant pyrazolopyrimidines (2).

Synthesis of prox-Benzoisoallopurinol

Foster, Robert H.,Leonard, Nelson J.

, p. 3072 - 3077 (2007/10/02)

Pyrazoloquinazolin-9-one (prox-benzoisoallopurinol, 1), an extented analogue of 7-hydroxypyrazolopyrimidine (isoallopurinol, 2) and a potential dimensional probe for substrates of xanthine oxidase, has been synthesized by two independent routes.The title compound, prepared by elaboration of either a suitably substituted indazole or a quinazolinone, was found to be an active substrate for and an alternative-substrate inhibitor of xanthine oxidase.The product of enzymatic oxidation of prox-benzoisoallopurinol has been identified as the corresponding prox-benzoisoalloxanthine.

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