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Merck
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Documentos Principais

287512

Sigma-Aldrich

3-Aminophenylboronic acid monohydrate

98%

Sinônimo(s):

3-Aminobenzeneboronic acid

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About This Item

Fórmula linear:
H2NC6H4B(OH)2 · H2O
Número CAS:
Peso molecular:
154.96
Beilstein:
2936342
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

98%

Formulário

solid

pf

93-96 °C (lit.)

cadeia de caracteres SMILES

[H]O[H].Nc1cccc(c1)B(O)O

InChI

1S/C6H8BNO2.H2O/c8-6-3-1-2-5(4-6)7(9)10;/h1-4,9-10H,8H2;1H2

chave InChI

XAEOVQODHLLNKX-UHFFFAOYSA-N

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Aplicação

Reagent used for
  • Suzuki-Miyaura cross-coupling

Reagent used for Preparation of
  • Gram-positive antivirulence drugs and inhibitors of Streptococcus agalactiae Stk1
  • Regioisomer of Zaleplon (a sedative)
  • Amphiphilic random glycopolymer, which self-assemble to form nanoparticles, with potential as a glucose-sensitive matrix
  • Chemomechanical polymer that expands and contracts in blood plasma with high glucose selectivity

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Jing Zhang et al.
Journal of separation science, 40(5), 1107-1114 (2017-01-04)
Novel 3-aminophenylboronic acid functionalized poly(glycidyl methacrylate-co-ethylene dimethacrylate) microspheres were prepared for the solid-phase extraction of glycopeptides/glycoproteins. The adsorption efficiency, maximum adsorption capacity, and specific recognition of the microspheres to glycoprotein were investigated. The results indicated excellent adsorption of glycoproteins by
Gizem Ertürk Bergdahl et al.
Applied biochemistry and biotechnology, 189(2), 374-383 (2019-04-26)
A capacitive sensor was developed to analyze the presence and enzymatic activity of a model protease from standard solutions by following the degradation of the substrate in real time. The enzyme was chosen based on its specific digestion of the
Aishwarya Mahadevan et al.
Biosensors & bioelectronics, 92, 417-424 (2016-11-12)
An improved glycerol biosensor was developed via direct attachment of NAD
Mayalen Oxoby et al.
Bioorganic & medicinal chemistry letters, 20(12), 3486-3490 (2010-06-10)
A structure-activity relationship study from a screening hit and structure-based design strategy has led to the identification of bisarylureas as potent inhibitors of Streptococcus agalactiae Stk1. As this target has been directly linked to bacterial virulence, these inhibitors can be
Xingju Jin et al.
Biomacromolecules, 10(6), 1337-1345 (2009-04-29)
This study is devoted to developing amphiphilic, random glycopolymers based on phenylboronic acid, which self-assemble to form nanoparticles (NPs), as a glucose-sensitive agent. Maleimide-glucosamine was copolymerized with 3-acryl aminophenylboronic acid in methanol at 70 degrees C. Using the nanoprecipitation method

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