CAS 137297-51-9
:4,4,5,5-Tetramethyl-2-[2-(phenylmethoxy)ethyl]-1,3,2-dioxaborolane
Description:
4,4,5,5-Tetramethyl-2-[2-(phenylmethoxy)ethyl]-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane ring structure, which includes two boron atoms and a five-membered cyclic arrangement. This compound features a phenylmethoxy group, contributing to its potential applications in organic synthesis and medicinal chemistry. The presence of multiple methyl groups enhances its steric bulk, which can influence its reactivity and solubility in various solvents. The dioxaborolane moiety is known for its ability to participate in various chemical reactions, including Suzuki coupling, making it valuable in the formation of carbon-carbon bonds. Additionally, the compound's structure suggests potential for use in drug development or as a reagent in organic transformations. Its stability and reactivity can be affected by environmental factors such as temperature and pH. Overall, this compound exemplifies the versatility of boron-containing compounds in synthetic organic chemistry.
Formula:C15H23BO3
InChI:InChI=1S/C15H23BO3/c1-14(2)15(3,4)19-16(18-14)10-11-17-12-13-8-6-5-7-9-13/h5-9H,10-12H2,1-4H3
InChI key:InChIKey=OYZPNTSHCBHHOP-UHFFFAOYSA-N
SMILES:C(COCC1=CC=CC=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:- 4,4,5,5-Tetramethyl-2-[2-(phenylmethoxy)ethyl]-1,3,2-dioxaborolane
- 2-[2-(Benzyloxy)ethyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[2-(phenylmethoxy)ethyl]-
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Found 2 products.
2-(Benzyloxy)ethylboronic acid pinacol ester
CAS:Formula:C15H23BO3Purity:95%Color and Shape:LiquidMolecular weight:262.15232-(Benzyloxy)ethylboronic acid pinacol ester
CAS:<p>Versatile small molecule scaffold</p>Formula:C15H25BO4Purity:Min. 95%Molecular weight:280.17 g/mol

