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3364-82-7

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3364-82-7 Usage

Description

(4-Oxothiazolidin-2-ylidene)acetonitrile, also known as OTAN, is a chemical compound with the molecular formula C5H4N2OS. It is a highly reactive and versatile compound, commonly used in organic synthesis for the preparation of new pharmaceuticals, agrochemicals, and materials. OTAN has been studied for its potential antimicrobial and antiviral activities. It is also used as a building block in the synthesis of various heterocyclic compounds. OTAN possesses a thiazolidin-2-ylidene moiety, which imparts unique reactivity and functional group compatibility, making it a valuable intermediate in the synthesis of diverse chemical compounds. Overall, (4-Oxothiazolidin-2-ylidene)acetonitrile is an important chemical building block with versatile applications in industrial and medicinal chemistry.

Uses

Used in Pharmaceutical Industry:
(4-Oxothiazolidin-2-ylidene)acetonitrile is used as a chemical intermediate for the synthesis of new pharmaceuticals, due to its unique reactivity and functional group compatibility.
Used in Agrochemical Industry:
(4-Oxothiazolidin-2-ylidene)acetonitrile is used as a building block in the development of new agrochemicals, contributing to the creation of innovative products for agricultural applications.
Used in Material Science:
(4-Oxothiazolidin-2-ylidene)acetonitrile is used as a key component in the synthesis of various materials, enhancing their properties and expanding their potential uses.
Used in Antimicrobial and Antiviral Research:
(4-Oxothiazolidin-2-ylidene)acetonitrile is used as a subject of study for its potential antimicrobial and antiviral activities, with the aim of developing new treatments and preventive measures against infectious diseases.
Used in Heterocyclic Compound Synthesis:
(4-Oxothiazolidin-2-ylidene)acetonitrile is used as a versatile building block in the synthesis of various heterocyclic compounds, which are important in the fields of organic chemistry and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3364-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3364-82:
(6*3)+(5*3)+(4*6)+(3*4)+(2*8)+(1*2)=87
87 % 10 = 7
So 3364-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2OS/c6-2-1-5-7-4(8)3-9-5/h1H,3H2,(H,7,8)/b5-1+

3364-82-7SDS

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-oxo-1,3-thiazolidin-2-ylidene)acetonitrile

1.2 Other means of identification

Product number -
Other names 2-Cyanomethylenthiazolidin-4-on

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:3364-82-7 SDS

3364-82-7Relevant articles and documents

Synthesis and DNase I inhibitory properties of some 4-thiazolidinone derivatives

Kolarevi?, Ana,Ili?, Budimir S.,Koci?, Gordana,D?ambaski, Zdravko,?melcerovi?, Andrija,Bond?i?, Bojan P.

, p. 264 - 274 (2019)

Twelve new thiazolidinones were synthesized and, together with 41 previously synthesized thiazolidinones,?evaluated for inhibitory activity against deoxyribonuclease I (DNase I) in vitro. Ten compounds inhibited commercial bovine pancreatic DNase I with a

Reactions of transition metal carbonyl anions with 2-(1-bromoalkylidene) thiazolidin-4-ones: Halogenophilic attack or deprotonation

Sazonov,D?ambaski,Shtern,Markovi?,Beletskaya

experimental part, p. 29 - 33 (2011/02/25)

Bromophilic attack by the transition metal carbonyl anion, [Re(CO) 5]Na (pKa = 21.1), on 2-(1-bromoalkylidene)thiazolidin-4- ones is significantly faster than abstraction of an acidic lactam hydrogen (pKa ~17-18), when the

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