456764
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
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关于此项目
线性分子式:
HO2CC6H4B(OH)2
化学文摘社编号:
分子量:
165.94
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Quality Level
assay
≥95%
mp
243-247 °C (lit.)
functional group
carboxylic acid
SMILES string
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
Application
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。
Other Notes
含不定量的酸酐
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
相关内容
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 456764-10G | 04061832904573 |
| 456764-1G | 04061832341668 |