4-Chloro-2,3-dihydro-1-benzofuran is an organic compound characterized by its bicyclic structure, which consists of a benzene ring fused to a furan ring. The presence of a chlorine atom at the 4-position of the benzofuran structure contributes to its reactivity and potential applications in various chemical reactions. This compound typically exhibits properties associated with both aromatic and aliphatic systems, including moderate polarity due to the electronegative chlorine substituent. It may be utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, owing to its unique structural features. The dihydro form indicates that it has two hydrogen atoms added to the furan ring, which can influence its stability and reactivity. Additionally, its CAS number, 289058-20-4, allows for easy identification in chemical databases. Overall, 4-chloro-2,3-dihydro-1-benzofuran is a versatile compound with potential applications in various fields of chemistry.

4-chloro-2,3-dihydro-1-benzofuran

289058-20-4: 4-Chloro-2,3-dihydrobenzofuran, Benzofuran, 4-Chloro-2,3-Dihydro-, 4-Chloro-2,3-dihydro-1-benzofuran

4-Chloro-2,3-dihydrobenzofuran

4-Chloro-2,3-dihydrobenzofuran is a primary alcohol that is used as a catalyst in intramolecular cyclization reactions. It is functionalized with chlorine and can be converted to a chloride salt. This compound undergoes an intramolecular cyclization reaction to form a six-membered ring structure. The cyclization reaction does not require an acid or base catalyst and can be performed in the presence of water. 4-Chloro-2,3-dihydrobenzofuran is more reactive than benzene, which makes it useful for synthesizing other compounds that contain the six-membered ring structure.

CAS 289058-20-4: 4-chloro-2,3-dihydro-1-benzofuran

4-Chloro-2,3-dihydrobenzofuran

Ref: 54-OR81753

4-Chloro-2,3-dihydrobenzofuran

Ref: 3D-FC139002

Benzofuran, 4-chloro-2,3-dihydro-

Ref: IN-DA002X1E

4-Chloro-2,3-dihydrobenzofuran

Ref: 10-F696068