287512
3-Aminophenylboronic acid monohydrate
98%
Sinonimo/i:
3-Aminobenzeneboronic acid
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About This Item
Formula condensata:
H2NC6H4B(OH)2 · H2O
Numero CAS:
Peso molecolare:
154.96
Beilstein:
2936342
Numero MDL:
Codice UNSPSC:
12352103
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
98%
Stato
solid
Punto di fusione
93-96 °C (lit.)
Stringa SMILE
[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
XAEOVQODHLLNKX-UHFFFAOYSA-N
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Applicazioni
Reagent used for
Reagent used for Preparation of
- 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
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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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
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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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