287512
3-氨基苯硼酸 一水合物
98%
别名:
间氨基苯硼酸
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关于此项目
线性分子式:
H2NC6H4B(OH)2 · H2O
化学文摘社编号:
分子量:
154.96
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2936342
InChI
1S/C6H8BNO2.H2O/c8-6-3-1-2-5(4-6)7(9)10;/h1-4,9-10H,8H2;1H2
SMILES string
[H]O[H].Nc1cccc(c1)B(O)O
InChI key
XAEOVQODHLLNKX-UHFFFAOYSA-N
assay
98%
form
solid
Quality Level
Application
用于
用于制备
- Suzuki-Miyaura交叉偶联的试剂
用于制备
- 无乳链球菌（Streptococcus agalactiae） STK1革兰氏阳性抗毒药物和抑制剂的试剂
- Zaleplon的区域异构体（镇静剂）
- 两亲性随机糖聚合物，其可自组装形成纳米颗粒，具有作为葡萄糖敏感基质的潜力
- 化学机械聚合物，可在血浆中膨胀和收缩，具有高葡萄糖选择性
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A chemomechanical polymer that functions in blood plasma with high glucose selectivity.
George K Samoei et al.
Angewandte Chemie (International ed. in English), 45(32), 5319-5322 (2006-08-24)
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
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
Qianqian Guo et al.
Journal of biomaterials science. Polymer edition, 30(10), 815-831 (2019-05-03)
We reported on the fabrication of sugar-responsive nanogels covalently incorporated with 3-acrylamidophenylboronic acid (AAPBA) as glucose-recognizing moiety, 2-(acrylamido)glucopyranose (AGA) as biocompatible moiety, and boron dipyrromethene (BODIPYMA) as fluorescence donor molecule. The p(AAPBA-AGA-BODIPYMA) nanogels were synthesized via reversible addition-fragmentation chain transfer
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