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130820-63-2

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130820-63-2 Usage

Structure

Quinolinone derivative with a bromophenyl group attached to the 2-position of the quinolinone ring

Usage

Building block for the synthesis of various bioactive molecules in the pharmaceutical industry

Biological activities

Anti-inflammatory and anticancer properties

Enzyme inhibition

Moderate inhibitory activity against certain enzymes

Value in research

Valuable chemical for drug discovery and development due to its diverse biological activities

Check Digit Verification of cas no

The CAS Registry Mumber 130820-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130820-63:
(8*1)+(7*3)+(6*0)+(5*8)+(4*2)+(3*0)+(2*6)+(1*3)=92
92 % 10 = 2
So 130820-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12BrNO/c16-11-7-5-10(6-8-11)14-9-15(18)12-3-1-2-4-13(12)17-14/h1-8,14,17H,9H2

130820-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)-2,3-dihydro-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 2-(4-Bromophenyl)-2,3-dihydro-4(1H)-quinolinone

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:130820-63-2 SDS

130820-63-2Relevant articles and documents

Organometallic titanocene complex as highly efficient bifunctional catalyst for intramolecular Mannich reaction

Wang, Yunyun,Jian, Yajun,Wu, Ya,Sun, Huaming,Zhang, Guofang,Zhang, Weiqiang,Gao, Ziwei

, (2019/05/07)

Bifunctional catalysts bearing two catalytic sites, Lewis acidic organometallic titanocene and Br?nsted acidic COOH, have been assembled in situ from Cp2TiCl2 with carboxylic acid ligands, showing high catalytic activity over an intramolecular Mannich reaction towards synthesis of 2-aryl-2,3-dihydroquinolin-4(1H)-ones. The determination of the bifunctional catalyst Cp2Ti(C8H4NO6)2 was elucidated by single X-ray HR-MS and investigation of catalytic behavior. In particular, masking the Br?nsted acidic COOH catalytic site with dormant COOMe lowered the reaction yield greatly, indicating that two catalytic sites work together to maintain high catalytic efficiency.

Titanocene complex with oxygen-containing carboxylic acid as ligand as well as preparation method and application of titanocene complex

-

Paragraph 0039; 0040; 0042, (2018/11/03)

The invention discloses a titanocene complex with oxygen-containing carboxylic acid as well as a preparation method and an application of the titanocene complex. The structural formula of the complexis shown in the description. The titanocene complex is p

Synthesis, molecular modeling and biological evaluation of aza-flavanones as α-glucosidase inhibitors

Kasturi, Sivaprasad,Surarapu, Sujatha,Bathoju, Chandra Chary,Uppalanchi, Srinivas,Dwivedi, Shubham,Perumal, Yogeeswari,Sigalapalli, Dilep Kumar,Babu, Bathini Nagendra,Ethiraj, Krishna S.,Anireddy, Jaya Shree

, p. 1618 - 1630 (2017/08/22)

An efficient acid catalyzed methodology has been employed to synthesize a variety of aza-flavanones and their α-glucosidase inhibitory activity is evaluated using acarbose, miglitol and voglibose as reference standards. Molecular modeling studies were per

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