CAS 18812-40-3

3-Thiophenecarboxaldehyde, 2-iodo-

Description:

3-Thiophenecarboxaldehyde, 2-iodo- 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 carboxaldehyde functional group (-CHO) attached to the thiophene ring at the 3-position and an iodine atom at the 2-position. This substitution pattern contributes to its unique reactivity and properties. The presence of the iodine atom can enhance the electrophilicity of the carbonyl carbon, making it more reactive in nucleophilic addition reactions. Additionally, the thiophene ring imparts aromatic stability and can participate in various chemical reactions, including electrophilic aromatic substitution. The compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals, agrochemicals, or other fine chemicals. Its physical properties, such as solubility and boiling point, are influenced by the functional groups and the aromatic nature of the thiophene ring. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

Formula: C₅H₃IOS

2-Iodothiophene-3-carbaldehyde

CAS: 18812-40-3

Formula: C₅H₃IOS

Purity: 95+%

Color and Shape: Solid

Molecular weight: 238.0462

Ref: IN-DA002GQD

2-Iodothiophene-3-carbaldehyde

CAS: 18812-40-3

Formula: C₅H₃IOS

Purity: 95.0%

Molecular weight: 238.04

Ref: 10-F362352

2-Iodothiophene-3-carbaldehyde

CAS: 18812-40-3

Versatile small molecule scaffold

Formula: C₅H₃IOS

Purity: Min. 95%

Molecular weight: 238.05 g/mol

Ref: 3D-TAA81240