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4-Carboxyphenylboronic acid_Molecular_structure_CAS_14047-29-1)
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4-Carboxyphenylboronic acid

Catalog No. 456772 Name Sigma Aldrich
CAS Number 14047-29-1 Website http://www.sigmaaldrich.com
M. F. C7H7BO4 Telephone 1-800-521-8956
M. W. 165.93908 Fax
Purity Email
Storage Chembase ID: 2840

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.)
MSDS Link Download
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

REFERENCES