456772
4-Carboxyphenylboronic acid
Synonym(s):
4-(Dihydroxyboronyl)benzoic acid, 4-(Dihydroxyboryl)benzoic acid, 4-Boronobenzoic acid, 4-Carboxybenzeneboronic acid, 4-Carboxylphenylboronic acid, 4-Hydroxycarbonylphenyl boronic acid, NSC 221170, p-Boronobenzoic acid, p-Carboxybenzeneboronic acid, p-Carboxyphenylboronic acid
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About This Item
Linear Formula:
HO2CC6H4B(OH)2
CAS Number:
Molecular Weight:
165.94
Beilstein:
3031088
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
EC Index Number:
604-189-6
NACRES:
NA.22
Quality Level
mp
220 °C (dec.) (lit.)
functional group
carboxylic acid
SMILES string
OB(O)c1ccc(cc1)C(O)=O
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
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Related Categories
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
Reagent used for
Reagent used in Preparation of
- 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
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Xiu Ye et al.
Nanomaterials (Basel, Switzerland), 9(5) (2019-05-10)
Aggregation-induced emission (AIE) active cellulose nanocrystals (TPE-CNCs) were synthesized by attaching tetraphenylethylene (TPE) to cellulose nanocrystals (CNCs). The structure and morphology of TPE-CNCs were characterized by FT-IR, XRD, ζ-potential measurements, elemental analysis, TEM, atomic force microscopy (AFM), and dynamic laser
Hai Wang et al.
Journal of colloid and interface science, 590, 103-113 (2021-02-02)
The self-healing mechanism and bioelectrochemical interface properties of supramolecular gels have been rarely explored. In this context, we propose a constitutive "fibril-reorganization" model to reveal the self-healing mechanism of a series of core-shell structured guanosine-borate (GB) hydrogels and emphasize that
Synthesis and biological evaluation of novel amprenavir-based P1-substituted bi-aryl derivatives as ultra-potent HIV-1 protease inhibitors
Yan, J.; et al.
Bioorganic & Medicinal Chemistry Letters, 22, 784-788 (2012)
Kentaro Yoshida et al.
Polymers, 12(8) (2020-08-23)
Phenylboronic acid-bearing polyamidoamine dendrimer (PBA-PAMAM)/poly(vinyl alcohol) (PVA) multilayer films were prepared through the layer-by-layer (LbL) deposition of PBA-PAMAM solution and PVA solution. PBA-PAMAM/PVA films were constructed successfully through the formation of boronate ester bonds between the boronic acid moiety in
Muthusamy Selvaraj et al.
Analytica chimica acta, 1066, 112-120 (2019-04-28)
A new boronic acid derivative functionalized with a 4-(3-(4-(4,5-diphenyl-1H-imidazole-2-yl)phenyl)-1,2,4-oxadiazol-5-yl)phenyl (IOP) moiety was synthesized for use as a sequential "on-off-on"-type relay fluorescence probe for Fe3+ ions and F- ions with high selectivity and sensitivity under physiological conditions. The introduction of Fe3+
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