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948552-89-4

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948552-89-4 Usage

General Description

6-Hydroxy-3,4-dihydroquinazolin-2(1H)-one is a chemical compound with the molecular formula C10H10N2O2. It is a derivative of the quinazolinone class of compounds and contains a hydroxyl group at the 6th position and a 3,4-dihydroquinazolin-2(1H)-one structure. 6-Hydroxy-3,4-dihydroquinazolin-2(1H)-one has potential pharmacological properties and has been studied for its potential applications in various fields, including medicinal chemistry and drug development. Its structure and properties make it a promising candidate for further research and development into its potential uses in pharmaceuticals and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 948552-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,5,5 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 948552-89:
(8*9)+(7*4)+(6*8)+(5*5)+(4*5)+(3*2)+(2*8)+(1*9)=224
224 % 10 = 4
So 948552-89-4 is a valid CAS Registry Number.

948552-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Hydroxy-3,4-dihydroquinazolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 6-hydroxy-3,4-dihydro-1H-quinazolin-2-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:948552-89-4 SDS

948552-89-4Downstream Products

948552-89-4Relevant articles and documents

An investigation leading to preparation of tetrahydro-quinazoline derivatives involving ureidoalkylation and α-amidoalkylation reactions

Pandey,Mukesh,Kumar, Anilesh,Trivedi, Noopur

experimental part, p. 1910 - 1914 (2009/05/30)

Reaction of an aldehyde with excess equivalent of urea in ethanol affords alkylideno/arylideno-bis-ureas 1 which on condensation with p-aminophenol in acidic medium cyclised to 4-aralkyl-6-hydroxy-2-oxo-1,2,3,4- tetrahydroquinazolines 2. Reaction of 2 with arylamidoalcohols in concentrated H2SO4 results in 4-arylkyl-7-arylamido/imidoalkyl-6- hydroxy-2-oxo-1,2,3,4-tetrahydroquinazolines 3, Compounds 3 have been evaluated for their effect on central nervous system (CNS) and cardiovascular system (CVS).

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