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25514-11-8

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25514-11-8 Usage

Chemical Class

Dihydroquinazolinones

Structural Features

Chlorine atom at the 6th position
Ethyl group at the 3rd position
Hydroxy group and phenyl group at the 4th position of the quinazolinone ring

Pharmaceutical Applications

Potential drug candidate for various biological activities

Synthetic Utility

Building block in organic synthesis for the development of new chemical entities

Significance in Research

Valuable compound for research and development in medicinal chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 25514-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,1 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25514-11:
(7*2)+(6*5)+(5*5)+(4*1)+(3*4)+(2*1)+(1*1)=88
88 % 10 = 8
So 25514-11-8 is a valid CAS Registry Number.

25514-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-3-ethyl-4-hydroxy-4-phenyl-1H-quinazolin-2-one

1.2 Other means of identification

Product number -
Other names 6-chloro-3-ethyl-4-hydroxy-4-phenyl-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:25514-11-8 SDS

25514-11-8Relevant articles and documents

The behaviour of 2-alkylamino- or dialkylamino-derivatives, respectively, of 5-phenyl-1,3,4-benzotriazepines in acid solution

Schleuder, M.,Richter, P.,Brandner, Anke,Morgenstern O.

, p. 259 - 260 (2007/10/02)

The title compounds are treated by HCl (0.1 or 5 mol*l-1, respectively) under mild or drastic conditions, respectively, and the products of the cleavage are identified.This was followed by the same investigation of the identified or expected in

Synthetic studies on quinazoline derivatives. II. The reactions of 2-trichloro- and 2-trifluoroacetamidobenzophenones with primary amines

Yamamoto,Yamamoto

, p. 2135 - 2156 (2007/10/02)

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