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4-Carboxyphenylboronic acid

ALDRICH/456772

Synonym: 4-(Dihydroxyboronyl)benzoic acid; 4-(Dihydroxyboryl)benzoic acid; 4-Boronobenzoic acid; 4-Carboxybenzeneboronic acid; 4-Carboxylphenylboronic acid; 4-Carboxylphenylboronic acid; 4-Hydroxycarbonylphenyl boronic acid; NSC 221170; p-Boronobenzoic acid; p-Carboxybenzeneboronic acid; p-Carboxyphenylboronic acid

CAS Number: 14047-29-1
Empirical Formula (Hill Notation): C7H7BO4
Molecular Weight: 165.94
MDL Number: MFCD00151801
Linear Formula: HO2CC6H4B(OH)2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-456772-1G 1 g
$43.40
1/EA
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45-456772-10G 10 g
$374.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 456772-1G

 

InChI 1S/C7H7BO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,11-12H,(H,9,10)
InChI key SIAVMDKGVRXFAX-UHFFFAOYSA-N
mp 220 °C (dec.) (lit.)
SMILES string OB(O)c1ccc(cc1)C(O)=O
Application: Reactant involved in:
• Condensation reactions with stabilizer chains at the surface of polystyrene latex
• Suzuki coupling reactions
• Esterification
• Derivatization of polyvinylamine
• Synthesis of isotopically labeled mercury
• Functionalization of poly-SiNW for detection of dopamine
Application: Reagent used for
• Suzuki-Miyaura cross-coupling
• Induction of pH sensitivity on fluorescence lifetime of quantum dots by NIR fluorescent dyes
• Bio-supported palladium nanoparticles as phosphine-free catalyst for Suzuki reaction in water
• Chan-Lam-type Copper (Cu)-catalyzed S-arylation with aryl boronic acids at room temperature

Reagent used in Preparation of
• Isoquinolones via regioselective Suzuki-Miyaura cross-coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation
• Amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors
• Phenols via visible-light initiated aerobic oxidative hydroxylation of arylboronic acids using air as oxidant catalyzed by Ruthenium (Ru)-complex
• Glucose sensitive boronic acid-bearing block copolymers
• Trisulfonated calixarene upper-rim sulfonamido derivatives and their complexation with the trimethyllysine epigenetic mark
Packaging: 1, 10 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) Not applicable
Flash Point(C) Not applicable
mp 220 °C (dec.) (lit.)
UNSPSC 12352103

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