CAS 1182283-83-5
:(4-(3-chloropropoxy)phenyl)boronic acid
Description:
(4-(3-Chloropropoxy)phenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a 3-chloropropoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications including organic synthesis and medicinal chemistry. The presence of the chloropropoxy substituent can influence its solubility and reactivity, potentially enhancing its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. Additionally, the chlorinated alkyl group may impart specific biological activities or enhance the compound's interaction with biological targets. Overall, (4-(3-chloropropoxy)phenyl)boronic acid serves as a versatile building block in the development of pharmaceuticals and agrochemicals, reflecting the importance of boron-containing compounds in modern chemistry.
Formula:C9H12BClO3
Synonyms:- (4-(3-chloropropoxy)phenyl)boronic acid
- Boronic acid, B-[4-(3-chloropropoxy)phenyl]-
- B-[4-(3-Chloropropoxy)phenyl]boronic acid
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