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:
产品名称
3-羧基苯硼酸, ≥95%
InChI
1S/C7H7BO4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H,(H,9,10)
SMILES string
OB(O)c1cccc(c1)C(O)=O
InChI key
DBVFWZMQJQMJCB-UHFFFAOYSA-N
assay
≥95%
mp
243-247 °C (lit.)
functional group
carboxylic acid
Quality Level
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
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Acta biomaterialia, 96, 123-136 (2019-06-28)
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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
Novel rhodamine dyes via Suzuki coupling of xanthone triflates with arylboroxins
Calitree, B. D.; Detty, M. R.
Synlett, 89-92 (2010)
Heterocycles, 60, 1891-1897 (2003)
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