4-Carboxyphenylboronic acid pinacol ester

CAS : 180516-87-4

Ref. 3D-FC33232

Informations sur le produit

• Nom: 4-Carboxyphenylboronic acid pinacol ester
• Synonymes: 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

Description

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.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 248.08 g/mol
• Formule: C₁₃H₁₇BO₄
• Degré de pureté: Min. 95%
• Couleur/Forme: White Powder
• InChI: InChI=1S/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)
• Code InChI: InChIKey=IYDKBQIEOBXLTP-UHFFFAOYSA-N
• SMILES: CC1(C)OB(c2ccc(C(=O)O)cc2)OC1(C)C