CAS 475250-49-8
:2-[(4-Chlorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Description:
2-[(4-Chlorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane ring structure, which contains boron and oxygen atoms. This compound features a chlorophenyl group, contributing to its potential applications in medicinal chemistry and material science. The presence of the tetramethyl substituents enhances its stability and solubility in organic solvents. Typically, compounds like this exhibit properties such as moderate to high polarity, making them suitable for various chemical reactions, including cross-coupling reactions in organic synthesis. The chlorophenyl moiety may also impart specific electronic properties, influencing reactivity and interaction with biological targets. Additionally, the dioxaborolane structure is known for its ability to form stable complexes with nucleophiles, which can be advantageous in synthetic pathways. Overall, this compound's characteristics make it a valuable intermediate in the synthesis of more complex organic molecules.
Formula:C13H18BClO2
InChI:InChI=1S/C13H18BClO2/c1-12(2)13(3,4)17-14(16-12)9-10-5-7-11(15)8-6-10/h5-8H,9H2,1-4H3
InChI key:InChIKey=JDACVUOXXNUDGH-UHFFFAOYSA-N
SMILES:C(B1OC(C)(C)C(C)(C)O1)C2=CC=C(Cl)C=C2
Synonyms:- 1,3,2-Dioxaborolane, 2-[(4-chlorophenyl)methyl]-4,4,5,5-tetramethyl-
- 2-(4-Chlorobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 2-[(4-Chlorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Found 3 products.
2-(4-Chlorobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C13H18BClO2Purity:95%Color and Shape:SolidMolecular weight:252.54484-Chlorobenzylboronic acid pinacol ester
CAS:4-Chlorobenzylboronic acid pinacol esterFormula:C13H18BClO2Purity:97%Color and Shape: white to off-white solidMolecular weight:252.54g/mol2-(4-Chlorobenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C13H18BClO2Purity:95%Color and Shape:SolidMolecular weight:252.55


