CAS 95453-58-0
:2-Chloro-1,3-thiazole-5-carboxaldehyde
Description:
2-Chloro-1,3-thiazole-5-carboxaldehyde is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features a chloro substituent at the second position and an aldehyde functional group at the fifth position of the thiazole ring. It is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. The presence of the aldehyde group makes it reactive, particularly in condensation reactions and as a potential electrophile in various organic syntheses. The thiazole ring contributes to its biological activity, making it of interest in medicinal chemistry and agrochemical applications. Additionally, 2-Chloro-1,3-thiazole-5-carboxaldehyde may exhibit properties such as solubility in organic solvents and moderate stability under standard conditions, although it should be handled with care due to its potential reactivity and toxicity.
Formula:C4H2ClNOS
InChI:InChI=1/C4H2ClNOS/c5-4-6-1-3(2-7)8-4/h1-2H
InChI key:PKCBQQXHFIDIIG-UHFFFAOYSA-N
SMILES:c1c(C=O)sc(Cl)n1
Synonyms:- 2-Chloro-1,3-thiazole-5-carbaldehyde
- 5-Thiazolecarboxaldehyde, 2-chloro-
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2-Chloro-1,3-thiazole-5-carboxaldehyde
CAS:Formula:C4H2ClNOSPurity:98%Color and Shape:SolidMolecular weight:147.58282-Chloro-5-formylthiazole
CAS:2-Chlorothiazole-5-carbaldehydeFormula:C4H2ClNOSPurity:98%Molecular weight:147.582-Chloro-1,3-thiazole-5-carboxaldehyde
CAS:2-Chloro-1,3-thiazole-5-carboxaldehydeFormula:C4H2ClNOSPurity:98%Color and Shape:SolidMolecular weight:147.582782-Chlorothiazole-5-carbaldehyde
CAS:Formula:C4H2ClNOSPurity:97%Color and Shape:SolidMolecular weight:147.58




