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CAS 134892-19-6

:

1,1-Dimethylethyl 4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-propanoate

Description:
1,1-Dimethylethyl 4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-propanoate, with the CAS number 134892-19-6, is a chemical compound that belongs to the class of boron-containing compounds. It features a dioxaborolane ring, which is characterized by its five-membered cyclic structure containing boron and oxygen atoms. This compound is typically used in organic synthesis, particularly in reactions involving boron chemistry, such as in the formation of carbon-boron bonds. Its structure includes bulky substituents, which can influence its reactivity and steric properties, making it useful in various applications, including as a reagent in cross-coupling reactions. The presence of the dimethyl and propanoate groups contributes to its solubility and stability in organic solvents. Additionally, the compound may exhibit specific physical properties such as boiling and melting points, which are influenced by its molecular structure. Overall, this compound is significant in the field of synthetic organic chemistry, particularly in the development of new methodologies for carbon-carbon bond formation.
Formula:C13H25BO4
InChI:InChI=1S/C13H25BO4/c1-11(2,3)16-10(15)8-9-14-17-12(4,5)13(6,7)18-14/h8-9H2,1-7H3
InChI key:InChIKey=DAPLUUBGLVENFC-UHFFFAOYSA-N
SMILES:C(CC(OC(C)(C)C)=O)B1OC(C)(C)C(C)(C)O1
Synonyms:
  • 2-(t-Butoxycarbonyl)ethylboronic acid pinacol ester
  • 1,3,2-Dioxaborolane-2-propanoic acid, 4,4,5,5-tetramethyl-, 1,1-dimethylethyl ester
  • tert-Butyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate
  • 1,1-Dimethylethyl 4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-propanoate
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