所有图片(2)
别名:
μ-Carboxyphenylboronic acid, 3-(Dihydroxyborane)benzoic acid, 3-(Dihydroxyboryl)benzoic acid, 3-Boronobenzoic acid, 3-Carboxybenzeneboronic acid
线性分子式:
HO2CC6H4B(OH)2
推荐产品
质量水平
检测方案
≥95%
mp
243-247 °C (lit.)
SMILES字符串
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 key
DBVFWZMQJQMJCB-UHFFFAOYSA-N
应用
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。
其他说明
含不定量的酸酐
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
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.
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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
Synthesis of a phenylboronic acid-functionalized thermosensitive block copolymer and its application in separation and purification of vicinal-diol-containing compounds
Wang Y, et al.
Royal Society of Chemistry Advances, 6(85), 82309-82320 (2016)
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