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4(3H)-Quinazolinone, 2-chloro-6-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80195-33-1

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80195-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80195-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,9 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80195-33:
(7*8)+(6*0)+(5*1)+(4*9)+(3*5)+(2*3)+(1*3)=121
121 % 10 = 1
So 80195-33-1 is a valid CAS Registry Number.

80195-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-6-nitro-1H-quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-chloro-6-nitro-3H-quinazolin-4-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:80195-33-1 SDS

80195-33-1Relevant academic research and scientific papers

QUINAZOLINONES AS PROLYL HYDROXYLASE INHIBITORS

-

Page/Page column 61, (2011/02/18)

Quinazolinone compounds of formula (I) are described, which are useful as prolyl hydroxylase inhibitors. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by prolyl hydroxylase activity. Thus, the compounds may be administered to treat, e.g., anemia, vascular disorders, metabolic disorders, and wound healing.

Oxidative cyclocondensation of cyclic thio(seleno)ureas. 4. Electronic effects of the substituents and the medium

Mukarramov,Urakov,Shakhidoyatov

, p. 540 - 545 (2008/02/02)

We have studied the electronic effect of substituents, steric factors, the medium, and the nature of the oxidizing agent on oxidative cyclocondensation of 2-thioxo-4-quinazolone and its substituted derivatives. We have found that electron-donor substituents promote the reaction while electronacceptor substituents inhibit the reaction. 2006 Springer Science+Business Media, Inc.

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