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55022-23-6

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55022-23-6 Usage

Appearance

Yellow solid

Usage

Organic synthesis, reagent for chemical reactions

Industries

Pharmaceutical, agrochemical

Biological activities

Antioxidant, anti-inflammatory properties

Therapeutic potential

Compound of interest for potential therapeutic applications

Fluorescent properties

Demonstrated potential as a fluorescent dye

Research applications

Imaging and labeling in biological and chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 55022-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,2 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55022-23:
(7*5)+(6*5)+(5*0)+(4*2)+(3*2)+(2*2)+(1*3)=86
86 % 10 = 6
So 55022-23-6 is a valid CAS Registry Number.

55022-23-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-methylpyridin-2-ylidene)indene-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(1-methyl-1H-[2]pyridylidene)-indan-1,3-dione

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:55022-23-6 SDS

55022-23-6Downstream Products

55022-23-6Relevant articles and documents

Synthesis and pharmacological evaluation of 2-(2 and 4- pyridinyl)indane-1,3-diones and structuraly related compounds exerting potential anti-inflammatory and antitumoral activities

Robert-Piessard,Leblois,Courant,Baut,Petit

, p. 160 - 168 (2007/10/03)

Our on going work in the series of enamido-diketones issued from 2- azaarylindane-1,3-diones led us to synthesize and experiment N and C2- substituted derivatives of 2-(2 and 4-pyridinyl)indane-1,3-diones as well as of structurally related compounds resulting from the replacement of pyridine by quinoline and benzimidazole. Pharmacological evaluation of their anti- inflammatory activity (by inhibition of carrageenan foot edema) and their anticoagulant activity (by prothombin assay) led to the conclusion of the possibility of achieving a selective antiinflammatory effect. It has been previously established that anticoagulants are liable to exert a protective effect in the development of cancer metastasis. Nevertheless none of the six experimented 2-(pyridin-2-yl)indane-1,3-diones extended survival time of mice treated by P388 lymphocytic leukemia.

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