跳转至内容
Merck

456764

Sigma-Aldrich

3-羧基苯硼酸

≥95%

别名:

μ-Carboxyphenylboronic acid, 3-(Dihydroxyborane)benzoic acid, 3-(Dihydroxyboryl)benzoic acid, 3-Boronobenzoic acid, 3-Carboxybenzeneboronic acid

登录查看公司和协议定价


About This Item

线性分子式:
HO2CC6H4B(OH)2
CAS号:
分子量:
165.94
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

化驗

≥95%

mp

243-247 °C (lit.)

SMILES 字串

OB(O)c1cccc(c1)C(O)=O

InChI

1S/C7H7BO4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H,(H,9,10)

InChI 密鑰

DBVFWZMQJQMJCB-UHFFFAOYSA-N

應用

3-羧基苯硼酸可用作制备以下物质的底物:
  • 二芳基衍生物(通过与溴苯胺的Suzuki-Miyaura偶联反应制备)
  • 硼酸功能化的嵌段共聚物
  • 1H-咪唑并[1,2-a]喹喔啉衍生物。

其他說明

含不定量的酸酐

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Christopher G Barber et al.
Bioorganic & medicinal chemistry letters, 14(12), 3227-3230 (2004-05-20)
A series of 1-isoquinolinylguanidines are shown to be potent inhibitors of uPA with selectivity over tPA and plasmin. Potency is enhanced by the presence of a 4-halo and a 7-aryl substituent, particularly when substituted by a 3-carboxylic acid group. Compound
Heterocycles, 60, 1891-1897 (2003)
Novel rhodamine dyes via Suzuki coupling of xanthone triflates with arylboroxins
Calitree, B. D.; Detty, M. R.
Synlett, 89-92 (2010)
Jumin Yang et al.
Materials science & engineering. C, Materials for biological applications, 116, 111250-111250 (2020-08-19)
Various nanoparticles as drug delivery system provide significant improvements in the cancer treatment. However, their clinical success remains elusive in large part due to their inability to overcome both systemic and tumor tissue barriers. The nanosystems with nanoproperty-transformability (surface, size
Identification and optimization of a novel series of indoleamine 2, 3-dioxygenase inhibitors
Markwalder JA, et al.
Bioorganic & Medicinal Chemistry Letters, 27(3), 582-585 (2017)

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门