CAS 180516-87-4

4-Carboxylphenylboronic acid pinacol ester

Description:

4-Carboxylphenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a carboxylic acid moiety attached to a phenyl ring. This compound typically exhibits a pinacol ester structure, which enhances its stability and solubility in organic solvents. The boronic acid functionality allows for reversible covalent bonding with diols, making it useful in various applications, including organic synthesis and materials science. The carboxyl group contributes to its acidity and potential reactivity in coupling reactions. Additionally, this compound may exhibit properties such as moderate polarity and the ability to participate in hydrogen bonding due to the presence of both the carboxylic acid and boronic acid functionalities. Its applications can extend to medicinal chemistry, particularly in the development of boron-containing drugs and as a building block in the synthesis of complex organic molecules. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₁₃H₁₇BO₄

InChI: InChI=1/C13H17BO4/c1-12(2)13(3,4)18-14(17-12)10-7-5-9(6-8-10)11(15)16/h5-8H,1-4H3,(H,15,16)

SMILES: CC1(C)C(C)(C)OB(c2ccc(cc2)C(=O)O)O1

Synonyms:

• 4-Carboxybenzeneboronic Acid Pinacol Cyclic Ester
• 4-Carboxyphenylboronic Acid Pinacolate
• 4-Carboxyphenylboronic Acid, Pinacol Cyclic Ester
• 4-Carboxyphenylboronic Acid, Pinacol Ester
• 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)benzoic acid
• [4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborinan-2-YL) benzoic acid]
• 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoicacid

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

CAS: 180516-87-4

Formula: C₁₃H₁₇BO₄

Purity: >98.0%(GC)(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 248.09

Ref: 3B-T2841

4-Carboxybenzeneboronic acid pinacol ester, 97%

CAS: 180516-87-4

4-Carboxybenzeneboronic acid pinacol ester is used to improvement of transition metal-mediated carbon-carbon as well as carbon-heteroatom cross-coupling reactions as a labeling feature with the focus on the preparation of radio labeled compounds for molecular imaging. This Thermo Scientific Chemical

Formula: C₁₃H₁₇BO₄

Purity: 97%

Color and Shape: White to pale cream, Crystals or powder or crystalline powder

Molecular weight: 248.09

Ref: 02-H26825

4-Carboxybenzeneboronic acid, pinacol ester

CAS: 180516-87-4

4-Carboxybenzeneboronic acid, pinacol ester

Formula: C₁₃H₁₇BO₄

Purity: 98%

Color and Shape: White Solid-Powder

Molecular weight: 248.08268

Ref: 54-OR10406

Benzoic acid, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

CAS: 180516-87-4

Formula: C₁₃H₁₇BO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 248.0827

Ref: IN-DA00222B

4-Carboxyphenylboronic acid pinacol ester

CAS: 180516-87-4

Formula: C₁₃H₁₇BO₄

Molecular weight: 248.08

Ref: 7W-GK1608

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

CAS: 180516-87-4

Formula: C₁₃H₁₇BO₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 248.09

Ref: 10-F010829

4-Carboxyphenylboronic acid pinacol ester

CAS: 180516-87-4

4-Carboxyphenylboronic acid pinacol ester is a linker that can be used to tether hydrophobic compounds to the surface of nanomaterials. This linker has been shown to have a low detection limit, meaning it can be used in red blood cells and cancer cells with high sensitivity. 4-Carboxyphenylboronic acid pinacol ester has also been shown to have an affinity for prostate cancer cells. The linker was synthesized from dopamine, which is a precursor molecule for many neurotransmitters in the central nervous system. It is important to note that this compound is not selective and can react with other hydrophilic molecules such as DNA or proteins.

Formula: C₁₃H₁₇BO₄

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 248.08 g/mol

Ref: 3D-FC33232