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19815-21-5

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19815-21-5 Usage

General Description

4,6,8-Trichloroquinazoline is a chemical compound that belongs to the quinazoline family. It is a trichlorinated derivative of quinazoline and is used as an intermediate in the synthesis of pharmaceutical drugs and agrochemicals. 4,6,8-TRICHLOROQUINAZOLINE has three chlorine atoms attached to the quinazoline ring, which gives it unique chemical properties. 4,6,8-Trichloroquinazoline is mainly used in the production of various pharmaceuticals, and it is also employed as a building block in the synthesis of other organic compounds. It is important to handle and store this chemical with proper safety precautions due to its reactivity and potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 19815-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19815-21:
(7*1)+(6*9)+(5*8)+(4*1)+(3*5)+(2*2)+(1*1)=125
125 % 10 = 5
So 19815-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H3Cl3N2/c9-4-1-5-7(6(10)2-4)12-3-13-8(5)11/h1-3H

19815-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6,8-trichloroquinazoline

1.2 Other means of identification

Product number -
Other names 4.6.8-Trichlorchinazolin

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:19815-21-5 SDS

19815-21-5Downstream Products

19815-21-5Relevant articles and documents

Microwave assisted synthesis of N-arylheterocyclic substituted-4- aminoquinazoline derivatives

Liu, Gang,Yang, Song,Song, Baoan,Xue, Wei,Hu, Deyu,Jin, Linhong,Lu, Ping

, p. 272 - 278 (2006)

A simple, efficient, and general method has been developed for the synthesis of various N-aryl heterocylic substituted-4-aminoquinazoline compounds from 4-chloro-quinazoline and aryl heterocyclic amines under microwave irradiation using 2-propanol as solvent. The advantages of the use of microwave irradiation in relation to the classical method were demonstrated.

Quinazolines, their preparation and biological activity

Schonowsky,Sachse

, p. 907 - 911 (2007/10/02)

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