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66301-15-3

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66301-15-3 Usage

General Description

2,5-dihydroxy-3-(piperidin-1-yl)-6-(pyridin-1(2H)-yl)cyclohexa-2,5-diene-1,4-dione is a chemical compound with potential biomedical applications. It is a synthetic compound that contains a piperidine ring and a pyridine ring, making it a heterocyclic compound. 2,5-dihydroxy-3-(piperidin-1-yl)-6-(pyridin-1(2H)-yl)cyclohexa-2,5-diene-1,4-dione has demonstrated potential as a pharmaceutical agent, particularly in the field of anti-cancer and anti-inflammatory drug development. Its structure and properties make it a promising candidate for further study and potential use in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 66301-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66301-15:
(7*6)+(6*6)+(5*3)+(4*0)+(3*1)+(2*1)+(1*5)=103
103 % 10 = 3
So 66301-15-3 is a valid CAS Registry Number.

66301-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dioxo-2,5-di(pyridin-1-ium-1-yl)cyclohexa-1,4-diene-1,4-diolate

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:66301-15-3 SDS

66301-15-3Downstream Products

66301-15-3Relevant articles and documents

Photocatalytically active materials with pyridinium-enolate partial structures

Schmidt, Andreas,Albrecht, Marcel

, p. 465 - 472 (2008)

2,3-Dichloro-1,4-naphthoquinone and tetrabromo- or tetrachloro-1,4- benzoquinone were converted into pyridinium enolate betaines by reaction with pyridine or 4,4′-bipyridine. The reaction conditions were applied to poly-(4-vinylpyridine) and a modified Me

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