CAS 214360-76-6

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Description:

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, with the CAS number 214360-76-6, is an organic compound that features a phenolic structure substituted with a dioxaborolane moiety. This compound is characterized by its boron-containing dioxaborolane ring, which contributes to its unique reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The presence of the tetramethyl groups enhances its stability and solubility in organic solvents. As a phenol derivative, it exhibits typical phenolic properties, such as the ability to act as a weak acid and participate in hydrogen bonding. The compound may also exhibit interesting optical properties due to its aromatic system. Its applications may extend to materials science, pharmaceuticals, and as a reagent in various chemical transformations. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards associated with its use.

Formula: C₁₂H₁₇BO₃

InChI: InChI=1S/C12H17BO3/c1-11(2)12(3,4)16-13(15-11)9-6-5-7-10(14)8-9/h5-8,14H,1-4H3

InChI key: InChIKey=MUKIFYQKIZOYKT-UHFFFAOYSA-N

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

Synonyms:

• 2-(3-Hydroxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• 3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
• 3-Hydroxyphenylboronic acid pinacol ester
• 3-Hydroxyphenylboronic acid,Pinacol cyclic ester
• Phenol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
• 3-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)phenol
• 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

CAS: 214360-76-6

Formula: C₁₂H₁₇BO₃

Purity: >98.0%(GC)

Color and Shape: White to Gray to Brown powder to crystal

Molecular weight: 220.08

Ref: 3B-T1953

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, min. 97%

CAS: 214360-76-6

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, min. 97%

Formula: C₁₂H₁₇BO₃

Purity: min. 97%

Color and Shape: pale yellow pwdr.

Molecular weight: 220.08

Ref: 08-05-1043

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

CAS: 214360-76-6

Formula: C₁₂H₁₇BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 220.0726

Ref: IN-DA003I2V

3-Hydroxybenzeneboronic acid, pinacol ester

CAS: 214360-76-6

3-Hydroxybenzeneboronic acid, pinacol ester

Formula: C₁₂H₁₇BO₃

Purity: 98%

Color and Shape: white to off-white solid

Molecular weight: 220.07g/mol

Ref: 54-OR11013

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

CAS: 214360-76-6

Formula: C₁₂H₁₇BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 220.08

Ref: 10-F010836

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

CAS: 214360-76-6

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a boronic acid that can be used as a starting material for the synthesis of chromanones. It is used in the Suzuki coupling reaction with boronic acids to produce functionalized biaryl compounds. This compound has been investigated by spectroscopies such as NMR and IR and was found to have a sequence of C8H8O. The phenol group in this molecule is oxidized to yield an alcohol. 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol has been shown to react with diaryliodonium salts and esters in order to form monomers for polymer synthesis.

Formula: C₁₂H₁₇BO₃

Purity: Min. 95%

Molecular weight: 220.08 g/mol

Ref: 3D-PIA36076