4-Carboxyphenylboronic acid

• Catalog No.: 456772
• CAS Number: 14047-29-1
• M. F.: C7H7BO4
• M. W.: 165.93908

SYNONYMS

• Title: 4-羧基苯硼酸
• IUPAC name: 4-(dihydroxyboranyl)benzoic acid
• IUPAC Traditional name: 4-carboxyphenylboronic acid
• Synonyms: 4-Carboxybenzeneboronic acid; 4-羧基苯基硼酸; NSC 221170; 4-(Dihydroxyboryl)benzoic acid; 4-(Dihydroxyboronyl)benzoic acid; 4-Boronobenzoic acid; 4-Carboxylphenylboronic acid; 4-Hydroxycarbonylphenyl boronic acid; p-Carboxybenzeneboronic acid; p-Carboxyphenylboronic acid; p-Boronobenzoic acid; 4-硼酸苯甲酸

DATABASE IDS

• PubChem SID: 24869234
• MDL Number: MFCD00151801
• Beilstein Number: 3031088
• CAS Number: 14047-29-1

PROPERTIES

• Linear Formula: HO2CC6H4B(OH)2
• Melting Point: 220 °C (dec.)(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• RTECS: CY8925000
• German water hazard class: 2

DETAILS

Description (English)

Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Condensation reactions with stabilizer chains at the surface of polystyrene latex1
• Suzuki coupling reactions2
• Esterification3
• Derivatization of polyvinylamine4
• Synthesis of isotopically labeled mercury5
• Functionalization of poly-SiNW for detection of dopamine6
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 temperatureReagent 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

Description (简体中文)

包装
1, 10 g in glass bottle
Application
Reactant involved in:
• Condensation reactions with stabilizer chains at the surface of polystyrene latex1
• Suzuki coupling reactions2
• Esterification3
• Derivatization of polyvinylamine4
• Synthesis of isotopically labeled mercury5
• Functionalization of poly-SiNW for detection of dopamine6
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 temperatureReagent 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