CAS 873077-21-5
:1,3,2-Dioxaborolane, 2-(3-chloro-1-propenyl)-4,4,5,5-tetramethyl-
Description:
1,3,2-Dioxaborolane, 2-(3-chloro-1-propenyl)-4,4,5,5-tetramethyl- is a boron-containing organic compound characterized by its unique dioxaborolane ring structure, which includes a five-membered cyclic arrangement featuring two oxygen atoms and a boron atom. This compound is notable for its potential applications in organic synthesis, particularly in the formation of carbon-boron bonds, which are valuable in various chemical reactions, including cross-coupling reactions. The presence of the 3-chloro-1-propenyl substituent enhances its reactivity, making it useful in further functionalization processes. Additionally, the tetramethyl groups contribute to the compound's steric bulk, influencing its reactivity and solubility properties. As with many boron compounds, it may exhibit unique electronic properties due to the presence of the boron atom, which can act as a Lewis acid. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.
Formula:C9H16BClO2
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2-(3-Chloroprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C9H16BClO2Molecular weight:202.4861
