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6134-99-2

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6134-99-2 Usage

Physical Appearance

White to light yellow crystalline powder

Molecular Weight

252.26 g/mol

Usage

Synthetic compound used in the manufacturing of pharmaceuticals, dyes, and other organic products

Precurser

Isatin is used as a precursor for the synthesis of various indole derivatives, which are important in medicinal and organic chemistry

Biological Activities

Antimicrobial, anticancer, and anti-inflammatory properties

Importance

Valuable compound in pharmaceutical research and development

Check Digit Verification of cas no

The CAS Registry Mumber 6134-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6134-99:
(6*6)+(5*1)+(4*3)+(3*4)+(2*9)+(1*9)=92
92 % 10 = 2
So 6134-99-2 is a valid CAS Registry Number.

6134-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylbenzoyl)indene-1,3-dione

1.2 Other means of identification

Product number -
Other names HMS1473C17

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:6134-99-2 SDS

6134-99-2Relevant articles and documents

Palladium-Catalyzed Carbonylative Annulation Reactions Using Aryl Formate as a CO Source: Synthesis of 2-Substituted Indene-1,3(2H)-dione Derivatives

Zhang, Ying,Chen, Jing-Lei,Chen, Zhen-Bang,Zhu, Yong-Ming,Ji, Shun-Jun

, p. 10643 - 10650 (2015/11/18)

An efficient synthesis of 2-substituted indene-1,3(2H)-diones from stable and readily available 1-(2-halophenyl)-1,3-diones by employing phenyl formate as a CO source has been developed. The reaction occurred via palladium-catalyzed intramolecular carbonylative annulation using K3PO4 as a base and DMSO as a solvent at 95 °C. In this protocol, the reaction showed a broad substrate scope with good to excellent yields.

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