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Merck
CN

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
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产品名称

3-氨基苯硼酸 一水合物, 98%

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

mp

93-96 °C (lit.)

Quality Level

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Application

用于
  • 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

pictograms

Exclamation mark

signalword

Warning

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


历史批次信息供参考:

分析证书(COA)

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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
Synthetic studies connected with the preparation of N-[3-(3-cyanopyrazolo[1,5-a]pyrimidin-5-yl)phenyl]-N-ethylacetamide, a zaleplon regioisomer
Radl, S.; et al.
Heterocycles, 80, 1359-1379 (2010)
Jiangying Zhu et al.
Materials science & engineering. C, Materials for biological applications, 117, 111273-111273 (2020-09-14)
In this work, poly(ethylene glycol)-b-poly[3-acrylamidophenylboronic acid-co-styrene] (PEG-b-P(PBA-co-St) has been firstly synthesized for loading of insulin to form insulin-loaded micelles. Insulin-loaded micelles (ILM) and epidermal growth factor (EGF) are further embedded into the composite hydrogels that can be rapidly gelled by
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
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

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