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2,3-Dihydrothiazolo[3,2-a]pyridinium-8-olate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23003-45-4

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23003-45-4 Usage

Molecular Structure

A complex molecule with a five-membered ring containing sulfur and nitrogen atoms, and a pyridine ring fused to the thiazole ring.

Classification

It belongs to the class of organic compounds known as thiazoles and is also classified as a pyridine derivative.

Charge

It is a positively charged ion known as a pyridinium salt, with the 8-olate anion providing the negative charge.

Usage

It is used in various chemical and pharmaceutical applications.

Research Interest

Its unique structure and properties make it of interest to researchers in the fields of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 23003-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,0 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23003-45:
(7*2)+(6*3)+(5*0)+(4*0)+(3*3)+(2*4)+(1*5)=54
54 % 10 = 4
So 23003-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NOS/c9-6-2-1-3-8-4-5-10-7(6)8/h1-3H,4-5H2

23003-45-4SDS

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 2,3-dihydro-[1,3]thiazolo[3,2-a]pyridin-4-ium-8-olate

1.2 Other means of identification

Product number -
Other names 2,3-dihydrothiazolo<3,2-a>pyridylium-8-olate

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:23003-45-4 SDS

23003-45-4Relevant academic research and scientific papers

1,3-Dipolar Character of Six-membered Aromatic Rings. Part 55. 3-Hydroxypyridine-2-thiones: Betaines, Cycloadditions, and Other Reactions

Katritzky, Alan R.,Grzeskowiak, Nicholas E.

, p. 2345 - 2389 (2007/10/02)

1-Methyl-2-methylthio-3-oxidopyridinium, 2-allylthio-1-methyl-3-oxidopyridinium, and 1--2-methylthio-3-oxidopyridinium undergo 1,3-dipolar cycloaddition to electron-deficient alkenes giving azabicyclooctene adducts having 1-alkylthio substituents.Quaternisation and tropone formation are investigated. 3-Hydroxypyridine-2-thione is cycloalkylated between sulphur and oxygen by substituted 1,1-dichloromethanes and certain α-haloacetyl chlorides. 1-(2-Pyridylmethyl)-3-oxidopyridinium gives azabicyclooctene cycloadducts with electron-deficient alkenes.The stereochemistry of all cycloadducts is deduced from the n.m.r.spectra.

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