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74246-64-3

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74246-64-3 Usage

Description

1,3-Thiazolin-4-one-2-acetonitrile, with the molecular formula C5H5N3OS, is a heterocyclic compound that features a thiazole ring fused with a ketone and an acetonitrile functional group. This unique structure endows it with distinctive chemical properties and reactivity, making it a versatile building block in organic synthesis.

Uses

Used in Pharmaceutical Industry:
1,3-Thiazolin-4-one-2-acetonitrile serves as a key building block for the synthesis of a variety of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications, making it a valuable asset in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1,3-thiazolin-4-one-2-acetonitrile is utilized as a precursor for the synthesis of various agrochemicals. Its ability to form a range of organic compounds contributes to the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Coordination Chemistry:
1,3-Thiazolin-4-one-2-acetonitrile has the potential to be employed as a ligand in coordination chemistry. Its interaction with metal ions can lead to the formation of coordination compounds with specific properties, useful in various applications such as catalysis and materials science.
Used as a Precursor for Bioactive Molecules:
Due to its reactivity and structural features, 1,3-thiazolin-4-one-2-acetonitrile can act as a precursor for the synthesis of bioactive molecules. These molecules may possess biological activities that can be harnessed in the development of new pharmaceuticals, agrochemicals, or other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 74246-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,4 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74246-64:
(7*7)+(6*4)+(5*2)+(4*4)+(3*6)+(2*6)+(1*4)=133
133 % 10 = 3
So 74246-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2OS/c6-2-1-5-7-4(8)3-9-5/h1,3H2

74246-64-3SDS

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 2-(4-oxo-1,3-thiazol-2-yl)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-cyanomethyl-2-thiazolin-4-one

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:74246-64-3 SDS

74246-64-3Relevant articles and documents

Synthesis of some new thiazolo[3,2-a]pyridines and related heterocyclic systems

Al-Thebeiti, Marzoog S.

, p. 109 - 118 (2000)

New 2,7-disubstituted 5-amino-6,8-dicyano-2,3-dihydro-3-oxo thiazolo[3,2-a]pyridines have been prepared. Their cyclization with formamide, nitrous acid and triethylorthoformate afforded a series of polycyclic heterocycles containing condensed pyrimidine and triazine rings. Antifungal tests were also performed. Copyright (C) 2000 Elsevier Science S.A.

Synthesis and Spectroscopic Studies on Some Dyes of the Type Dihydrazono 2-cyanomethyl-2-thiazolin-4-one

Shams, Hoda Z.,Khalifa, Fathy A.,Barsoum, Barsoum N.,Naoum, Magdi M.

, p. 119 - 122 (2007/10/02)

Several new dihydrazono-2-thiazolin-4-one dyes 6a-j are synthesized in excellent yields via coupling of 2-cyanomethyl-2-thiazolin-4-one 1 with diazotised aromatic amines in excess pyridine.Proofs of structures based on microanalytical and spectroscopic data are given and discussed.Electronic absorption spectra of the so synthesized dyes are studied in aqueous buffer solutions of varying pH, and their dissociation constants pK are determined spectrophotometrically.

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