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Merck
CN

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
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3030770
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产品名称

4-甲酰基苯硼酸, ≥95.0%

InChI

1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H

SMILES string

OB(O)c1ccc(C=O)cc1

InChI key

VXWBQOJISHAKKM-UHFFFAOYSA-N

assay

≥95.0%

mp

237-242 °C (lit.)

functional group

aldehyde

Quality Level

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Application

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。

Other Notes

含不定量的酸酐

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Sens. 1

存储类别

11 - Combustible Solids

wgk

WGK 1

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

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Suzuki?Miyaura coupling on the three upper rims of hexahomotrioxacalix[3]arenes
Tsubaki K, et al.
Tetrahedron, 62(44), 10321-10321 (2006)
Synthesis of Some New 1,4-Dihydropyridine Derivatives through a Facile One-pot Hantzsch Condensation Catalyzed by Triethylamine
Ghalem W, et al.
Chin. J. Chem., 30, 733-737 (2012)
Kunpeng Guo et al.
Organic letters, 14(9), 2214-2217 (2012-04-14)
This work identifies the dithiafulvenyl unit as an excellent electron donor for constructing D-π-A-type metal-free organic sensitizers of dye-sensitized solar cells (DSCs). Synthesized and tested are three sensitizers all with this donor and a cyanoacrylic acid acceptor but differing in
Shi-En Chen et al.
Analytica chimica acta, 1124, 40-51 (2020-06-15)
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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

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