CAS 2121511-69-9

2-[4-Chloro-3-(1-methylethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:

2-[4-Chloro-3-(1-methylethyl)phenyl]-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 exhibits a chloro-substituted phenyl group, contributing to its potential reactivity and applications in organic synthesis, particularly in cross-coupling reactions. The presence of the isopropyl group enhances its steric properties, which can influence its reactivity and solubility in various solvents. The dioxaborolane moiety is known for its ability to form stable complexes with nucleophiles, making it useful in the development of boron-based reagents. Additionally, compounds like this one may exhibit interesting biological activities, although specific biological data would require further investigation. Overall, this compound's structural features suggest it could serve as a valuable intermediate in synthetic chemistry, particularly in the fields of medicinal chemistry and materials science.

Formula: C₁₅H₂₂BClO₂

InChI: InChI=1S/C15H22BClO2/c1-10(2)12-9-11(7-8-13(12)17)16-18-14(3,4)15(5,6)19-16/h7-10H,1-6H3

InChI key: InChIKey=YCOKHZHJURWXMG-UHFFFAOYSA-N

SMILES: CC1(C)OB(OC1(C)C)C2=CC(C(C)C)=C(Cl)C=C2

Synonyms:

• 1,3,2-Dioxaborolane, 2-[4-chloro-3-(1-methylethyl)phenyl]-4,4,5,5-tetramethyl-
• 2-[4-Chloro-3-(1-methylethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1,3,2-Dioxaborolane, 2-[4-chloro-3-(1-methylethyl)phenyl]-4,4,5,5-tetramethyl-

CAS: 2121511-69-9

Formula: C₁₅H₂₂BClO₂

Purity: 97%

Molecular weight: 280.5980

Ref: IN-DA01RC8B

2-(4-Chloro-3-isopropylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS: 2121511-69-9

Purity: ≥95%

Molecular weight: 280.6000061

Ref: 10-F627685