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2-(4-methylpyridin-2(1H)-ylidene)-1H-indene-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71107-23-8

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71107-23-8 Usage

Molecular structure

Contains a pyridin-2(1H)-ylidene group and a 1H-indene-1,3(2H)-dione moiety.

Derivative

Of indene and pyridine.

Potential applications

In the pharmaceutical and chemical industries.

Possible use as a pharmacophore

Due to its ability to interact with biological targets.

Versatile intermediate

For the synthesis of other compounds with diverse properties and applications.

Further research and development

Could lead to innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 71107-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,0 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71107-23:
(7*7)+(6*1)+(5*1)+(4*0)+(3*7)+(2*2)+(1*3)=88
88 % 10 = 8
So 71107-23-8 is a valid CAS Registry Number.

71107-23-8SDS

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-(4-methyl-1H-pyridin-2-ylidene)indene-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-(4-Methyl-1H-[2]pyridyliden)-indan-1,3-dion

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:71107-23-8 SDS

71107-23-8Relevant academic research and scientific papers

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.

β-Diceto enamines heterocycliques: 1. Indanediones-1,3 substituees en 2 par un heterocycle azote

Ploquin, J.,Sparfel, L.,Baut, G. Le,Floc'h, R.,Letourneux, Y.

, p. 961 - 973 (2007/10/02)

The condensation of methylated N-heterocycles and especially monomethyl- and polymethylpyridines on phthalic anhydrides leads to 2-aryl-1,3-indanediones.The 3-alkylidenylphthalides formed in an intermediary state have been isolated.The influence of solvents and temperature on the velocity and yield of formation of 2-(2- and 4-pyridyl)-1,3-indandiones has been studied.The ir and nmr spectra confirm that these compounds exist under a β-diketoenamine form resonating with a betaine form.

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