CAS 61209-02-7
:2-Thiophenecarboxylic acid, 3,4-dichloro-
Description:
2-Thiophenecarboxylic acid, 3,4-dichloro- is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The compound features a carboxylic acid functional group (-COOH) attached to the thiophene ring, specifically at the 2-position, while two chlorine atoms are substituted at the 3 and 4 positions of the ring. This substitution pattern contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of chlorine atoms enhances the compound's electrophilicity and can influence its solubility and stability. As a carboxylic acid, it exhibits typical acid-base behavior, being capable of donating a proton in solution. The compound's molecular structure allows for various interactions, making it a candidate for further chemical modifications or as a building block in synthetic chemistry. Its CAS number, 61209-02-7, uniquely identifies it in chemical databases, facilitating research and regulatory considerations.
Formula:C5H2Cl2O2S
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Found 7 products.
3,4-Dichlorothiophene-2-carboxylic acid
CAS:Formula:C5H2Cl2O2SPurity:98%Color and Shape:SolidMolecular weight:197.03923,4-Dichlorothiophene-2-carboxylic acid
CAS:<p>3,4-Dichlorothiophene-2-carboxylic acid</p>Purity:98%Molecular weight:197.04g/mol3,4-Dichlorothiophene-2-carboxylic Acid
CAS:Controlled Product<p>Applications 3,4-Dichlorothiophene-2-carboxylic acid is a reagent used in the preparation of nicotinamides as PDE4 D isoenzymes inhibitors.<br>References Marfat, A. et al.: PCT Int. Appl., (1998)<br></p>Formula:C5H2Cl2O2SColor and Shape:NeatMolecular weight:197.0393,4-Dichlorothiophene-2-carboxylic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C5H2Cl2O2SPurity:Min. 95%Molecular weight:197.04 g/mol






