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700-78-7

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700-78-7 Usage

Synthesis Reference(s)

Tetrahedron, 62, p. 12351, 2006 DOI: 10.1016/j.tet.2006.09.103

Check Digit Verification of cas no

The CAS Registry Mumber 700-78-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 700-78:
(5*7)+(4*0)+(3*0)+(2*7)+(1*8)=57
57 % 10 = 7
So 700-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2/c9-7-1-2-8-6(3-7)4-10-5-11-8/h1-5H

700-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloroquinazoline

1.2 Other means of identification

Product number -
Other names 6-chloroquinazoline

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:700-78-7 SDS

700-78-7Relevant articles and documents

I2-catalyzed aerobic oxidative C(sp3)-H amination/C-N cleavage of tertiary amine: Synthesis of quinazolines and quinazolinones

Yan, Yizhe,Xu, Ying,Niu, Bin,Xie, Huifang,Liu, Yanqi

, p. 5581 - 5587 (2015/06/16)

An iodine-catalyzed oxidative C(sp3)-H amination/C-N cleavage of tertiary amines couducted under an oxygen atmosphere has been developed and affords a route to quinazolines and quinazolinones in good to excellent yields via a domino ring annulation. The method is metal-free, peroxide-free, and operationally simple to implement with a wide scope of substrates and represents a new avenue for multiple C-N bond formations.

NOVEL CHEMICAL COMPOUNDS

-

Page/Page column 27, (2010/11/26)

This invention relates to newly identified compounds for inhibiting hYAK3 proteins and methods for treating diseases associated with the imbalance or inappropriate activity of hYAK3 proteins.

A microwave improvement in the synthesis of the quinazoline scaffold

Chilin, Adriana,Marzaro, Giovanni,Zanatta, Samuele,Guiotto, Adriano

, p. 3229 - 3231 (2008/02/02)

A rapid and efficient microwave-assisted protocol is described that greatly improves a recent synthetic method developed for quinazoline synthesis. The synthetic protocol is based on the use of cycles of microwave irradiation. The optimization process is reported and the experimental results are compared with those of the conventional synthetic route.

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