431966
4-甲酰基苯硼酸
≥95.0%
别名:
4-醛基苯硼酸, 对甲酰苯硼酸
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关于此项目
线性分子式:
HCOC6H4B(OH)2
化学文摘社编号:
分子量:
149.94
Beilstein:
3030770
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
≥95.0%
mp
237-242 °C (lit.)
官能团
aldehyde
SMILES字符串
OB(O)c1ccc(C=O)cc1
InChI
1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
InChI key
VXWBQOJISHAKKM-UHFFFAOYSA-N
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应用
4-甲酰基苯硼酸是Suzuki交叉偶联反应的底物，用作以下应用的试剂：
- 钯催化的水中Suzuki-Miyaura交叉偶联。
- 芳基硼酸与氟烷基碘的铜介导无配体有氧氟烷基化。
- 硝基芳烃与芳基硼酸的无配体铜催化偶联。
- 三乙胺催化的三组分汉斯酯缩合物。
- 铜催化硝化。
- 毛栓菌催化二烯烃的氧化单裂解。
- 芳基硼酸与羧酸酐或酰氯的钯催化交叉偶联。
- 钯催化氧气氧化交叉偶联反应。
- 敏化剂与作为电子供体的二噻呋烯基单元的合成，用于高效染料敏化太阳能电池。
- 新型抗革兰氏阳性菌蛋白合成抑制剂的合成。
- hexahomotrioxacalix[3]芳烃上边缘的Suzuki芳香偶合反应。
- 铑催化环合作用，将1,5-烯炔转换为环戊烯和螺环戊烯。
其他说明
含不定量的酸酐
警示用语：
Warning
危险声明
危险分类
Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 1
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
A new and simple synthetic approach to functionalized sulphone derivatives by the Suzuki-Miyaura cross-coupling reaction
Kotha S and Ghosh AK
Indian J. Chem. B, 45(1), 227-231 (2006)
Nora R Eibergen et al.
Chembiochem : a European journal of chemical biology, 13(4), 574-583 (2012-03-01)
In an effort to identify novel antibacterial chemotypes, we performed a whole-cell screen for inhibitors of Staphylococcus aureus growth and pursued those compounds with previously uncharacterized antibacterial activity. This process resulted in the identification of a benzothiazolium salt, ABTZ-1, that
Palladacycle-catalyzed cross-coupling reactions of arylboronic acids with carboxylic anhydrides or acyl chlorides
Yu, A.; et al.
Tetrahedron, 68, 2283-2288 (2012)
Suzuki Coupling at the 2-Position of Densely Functionalized Pyrimidones
Colarusso, Stefania; et al.
Synthesis, 8, 1343-1350 (2006)
Caroline E Paul et al.
Chemical communications (Cambridge, England), 48(27), 3303-3305 (2012-02-24)
The first report of a biocatalytic regioselective oxidative mono-cleavage of dialkenes was successfully achieved employing a cell-free enzyme preparation from Trametes hirsuta at the expense of molecular oxygen. Selected reactions were performed on a preparative scale affording high to excellent
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