CAS 2120-82-3

3,5-Dichloro-1,2-thiazole-4-carbonitrile

Description:

3,5-Dichloro-1,2-thiazole-4-carbonitrile is a heterocyclic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features two chlorine substituents at the 3 and 5 positions of the thiazole ring, contributing to its reactivity and potential biological activity. The presence of a cyano group (-C≡N) at the 4 position enhances its chemical properties, making it useful in various synthetic applications. Typically, compounds like this exhibit moderate to high stability under standard conditions but may undergo hydrolysis or other reactions in the presence of strong acids or bases. 3,5-Dichloro-1,2-thiazole-4-carbonitrile is often utilized in the synthesis of agrochemicals, pharmaceuticals, and other organic compounds due to its ability to act as a building block in chemical reactions. Safety precautions should be observed when handling this compound, as halogenated compounds can pose health risks and environmental concerns.

Formula: C₄Cl₂N₂S

InChI: InChI=1/C4Cl2N2S/c5-3-2(1-7)4(6)9-8-3

SMILES: C(#N)c1c(Cl)nsc1Cl

Synonyms:

• 4-Isothiazolecarbonitrile, 3,5-dichloro-
• 3,5-Dichloro-4-Cyanoisothiazole
• 3,5-Dichloroisothiazole-4-Carbonitrile

3,5-Dichloroisothiazole-4-carbonitrile

CAS: 2120-82-3

Formula: C₄Cl₂N₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 179.0272

Ref: IN-DA007OS2

3,5-Dichloroisothiazole-4-carbonitrile

CAS: 2120-82-3

3,5-Dichloroisothiazole-4-carbonitrile

Purity: 95%

Molecular weight: 179.03g/mol

Ref: 54-OR1072368

3,5-Dichloroisothiazole-4-carbonitrile

CAS: 2120-82-3

Formula: C₄Cl₂N₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 179.02

Ref: 10-F209795

3,5-Dichloroisothiazole-4-carbonitrile

CAS: 2120-82-3

3,5-Dichloroisothiazole-4-carbonitrile is used as a reagent in organic synthesis. It is a regiospecifically chlorinated derivative of 3,5-dichloroisonicotinamide that can be prepared by reacting ethyl bromoacetate with chlorosulfonyl isocyanate. This compound reacts with phenols to give 3-chloro-1,2,4-benzothiadiazoles and other products. The reaction is catalysed by alkalis and reactive chlorine compounds such as chlorine gas or chlorosulfonic acid. 3,5-Dichloroisothiazole-4-carbonitrile also reacts with amines to give amides. 3,5-Dichloroisothiazole-4-carbonitrile reacts with halogens to form alkyl halides or alkyl sulfonates.

Formula: C₄Cl₂N₂S

Purity: Min. 95 Area-%

Color and Shape: Powder

Molecular weight: 179.03 g/mol

Ref: 3D-FD141510