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4-Chloro-7-(4-fluorophenyl)quinazoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1197199-75-9

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1197199-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197199-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,1,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1197199-75:
(9*1)+(8*1)+(7*9)+(6*7)+(5*1)+(4*9)+(3*9)+(2*7)+(1*5)=209
209 % 10 = 9
So 1197199-75-9 is a valid CAS Registry Number.

1197199-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-7-(4-fluorophenyl)quinazoline

1.2 Other means of identification

Product number -
Other names -

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:1197199-75-9 SDS

1197199-75-9Relevant academic research and scientific papers

Quinazoline sulfonamides as dual binders of the proteins B-cell lymphoma 2 and B-cell lymphoma extra long with potent proapoptotic cell-based activity

Sleebs, Brad E.,Czabotar, Peter E.,Fairbrother, Wayne J.,Fairlie, W. Douglas,Flygare, John A.,Huang, David C. S.,Kersten, Wilhelmus J. A.,Koehler, Michael F. T.,Lessene, Guillaume,Lowes, Kym,Parisot, John P.,Smith, Brian J.,Smith, Morey L.,Souers, Andrew J.,Street, Ian P.,Yang, Hong,Baell, Jonathan B.

experimental part, p. 1914 - 1926 (2011/05/30)

ABT-737 and ABT-263 are potent inhibitors of the BH3 antiapoptotic proteins, Bcl-xL and Bcl-2. This class of putative anticancer agents invariantly contains an acylsulfonamide core. We have designed and synthesized a series of novel quinazoline-based inhibitors of Bcl-2 and Bcl-xL that contain a heterocyclic alternative to the acylsulfonamide. These compounds exhibit submicromolar, mechanism-based activity in human small-cell lung carcinoma cell lines in the presence of 10% human serum. This comprises the first successful demonstration of a quinazoline sulfonamide core serving as an effective benzoylsulfonamide bioisostere. Additionally, these novel quinazolines comprise only the second known class of Bcl-2 family protein inhibitors to induce mechanism-based cell death.

ARYLSULFONAMIDE COMPOUNDS, COMPOSITIONS AND METHODS OF USE

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Page/Page column 224, (2009/12/27)

Disclosed are compounds which inhibit the activity of anti-apoptotic protein family members, compositions containing the compounds and uses of the compounds for preparing medicaments for treating diseases during which occurs expression one or more than one of an anti apoptotic protein family member.

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