
CAS 2121513-78-6
:2-(3-Chloro-2,4-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Description:
2-(3-Chloro-2,4-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound is notable for its potential applications in organic synthesis and medicinal chemistry, particularly as a reagent in cross-coupling reactions. The presence of the chloro and dimethyl groups on the phenyl ring contributes to its reactivity and solubility properties, making it suitable for various chemical transformations. The tetramethyl substituents enhance the stability of the dioxaborolane ring, which is crucial for its function in synthetic pathways. Additionally, the compound's molecular structure suggests it may exhibit interesting electronic properties, potentially influencing its behavior in chemical reactions. Overall, this compound exemplifies the versatility of boron compounds in organic chemistry, particularly in the development of new synthetic methodologies.
Formula:C14H20BClO2
InChI:InChI=1S/C14H20BClO2/c1-9-7-8-11(10(2)12(9)16)15-17-13(3,4)14(5,6)18-15/h7-8H,1-6H3
InChI key:InChIKey=WHRKUIRRZFYHSP-UHFFFAOYSA-N
SMILES:CC1=C(B2OC(C)(C)C(C)(C)O2)C=CC(C)=C1Cl
Synonyms:- 2-(3-Chloro-2,4-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 1,3,2-Dioxaborolane, 2-(3-chloro-2,4-dimethylphenyl)-4,4,5,5-tetramethyl-
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3-Chloro-2,4-dimethylphenylboronic acid pinacol ester
CAS:3-Chloro-2,4-dimethylphenylboronic acid pinacol esterFormula:C14H20BClO2Molecular weight:266.573-Chloro-2,4-dimethylphenylboronic acid pinacol ester
CAS:Formula:C14H20BClO2Purity:95%Molecular weight:266.5714



