| Identification | More | [Name]
4-Carboxyphenylboronic acid | [CAS]
14047-29-1 | [Synonyms]
4-BORONOBENZOIC ACID
4-CARBOXYBENZENEBORONIC ACID
4-CARBOXYPHENYLBORONIC ACID
4-(DIHYDROXYBORANE)BENZOIC ACID
4-(DIHYDROXYBORYL)BENZOIC ACID
AKOS BRN-0008
AURORA 14935
IFLAB-BB F1371-0202
OTAVA-BB BB7110951390
P-CARBOXYPHENYLBORONIC ACID
RARECHEM AH PB 0147
TIMTEC-BB SBB003899
ZERENEX ZX001647
4-borono-benzoicaci
p-borono-benzoicaci
p-boronobenzoicacid
p-carboxy-benzeneboronicaci
p-carboxybenzeneboronicacid
4-(Dihydroxyboronyl)benzoic acid
4-Carboxypenylboronic Acid | [EINECS(EC#)]
604-189-6 | [Molecular Formula]
C7H7BO4 | [MDL Number]
MFCD00151801 | [Molecular Weight]
165.94 | [MOL File]
14047-29-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Off-white to light beige powder | [Melting point ]
220 °C (dec.) (lit.) | [Boiling point ]
406.4±47.0 °C(Predicted) | [density ]
1.40±0.1 g/cm3(Predicted) | [storage temp. ]
0-6°C | [solubility ]
DMSO (Slightly), Methanol (Slightly), Water (Slightly) | [form ]
Powder | [pka]
4.08±0.10(Predicted) | [color ]
Off-white to light beige | [Usage]
Intermediates of Liquid Crystals | [Detection Methods]
HPLC,NMR | [BRN ]
3031088 | [InChI]
InChI=1S/C7H7BO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4,11-12H,(H,9,10) | [InChIKey]
SIAVMDKGVRXFAX-UHFFFAOYSA-N | [SMILES]
C(O)(=O)C1=CC=C(B(O)O)C=C1 | [CAS DataBase Reference]
14047-29-1(CAS DataBase Reference) |
| Questions And Answer | Back Directory | [Description]
4-Carboxyphenylboronic acid is a highly versatile reagent. It is a reagent used in various reactions including condensation reactions with stabilizer chains at the surface of polystyrene latex, Suzuki coupling reactions, esterification, derivatization of polyvinylamine, synthesis of isotopically labeled mercury and functionalization of poly-SiNW for detection of dopamine. It is reagents 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 and Chan-Lam-type Copper (Cu)-catalyzed S-arylation with aryl boronic acids at room temperature. It is reagents used for the 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. It can also be used as a corrosion inhibitor for steel.
| [Reference]
- Nam, N. D., et al. "A study of 4-carboxyphenylboronic acid as a corrosion inhibitor for steel in carbon dioxide containing environments." Corrosion Science 76.10(2013):257-266.
- Vollmueller, Frank, et al. "Cyclization of 4-carboxyphenylboronic acid with hydrazide derivative; hydrolysis; catalytic esterification." US, US 6197967 B1. 2001.
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CE Pharm Co.,Ltd Gold
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15317222985 |
| Website: |
www.cepharm.cn/ |
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J & K SCIENTIFIC LTD.
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18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Alfa Aesar
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400-6106006 |
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http://chemicals.thermofisher.cn |
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Energy Chemical
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400-0056266 |
| Website: |
www.energy-chemical.com |
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