跳转至内容
Merck
CN

513016

Sigma-Aldrich

3-氰基苯硼酸

≥95.0%

登录查看公司和协议定价

别名:
(m-Cyanophenyl)boronic acid, 3-Cyanobenzeneboronic acid
线性分子式:
NCC6H4B(OH)2
分子量:
146.94
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥95.0%

mp

298 °C (dec.) (lit.)

SMILES字符串

OB(O)c1cccc(c1)C#N

InChI

1S/C7H6BNO2/c9-5-6-2-1-3-7(4-6)8(10)11/h1-4,10-11H

InChI key

XDBHWPLGGBLUHH-UHFFFAOYSA-N

应用

3-Cyanophenylboronic acid can be used:
  • As an intermediate in the synthesis of piperidine-based MCH R1 antagonists.
  • As a substrate in the Suzuki coupling reactions to prepare 4-aryl-1,8-naphthyridin-2(1H)-ones.
  • As an intermediate in the synthesis of biaryl-based phenylalanine amino acid analogs, which are used as kainate receptors ligands.
  • To prepare phenylimidazole-based Ir(III) complexes for phosphorescent blue OLED applications.

其他说明

含有不定量的酸酐

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

A convenient synthesis of 4-aryl-1, 8-naphthyridin-2 (1H)-ones by the Suzuki coupling
Ban H, et al.
Tetrahedron Letters, 44(32), 6021-6023 (2003)
Synthesis and structure-activity relationships of piperidine-based melanin-concentrating hormone receptor 1 antagonists
Wu W-L, et al.
Bioorganic & medicinal chemistry letters, 16(14), 3668-3673 (2006)
Design, synthesis and structure-activity relationships of novel phenylalanine-based amino acids as kainate receptors ligands
Szyma'nska E, et al.
Bioorganic & Medicinal Chemistry Letters, 26(22), 5568-5572 (2016)
Functionalized phenylimidazole-based facial-homoleptic iridium (III) complexes and their excellent performance in blue phosphorescent organic light-emitting diodes
Kwon Y, et al.
Journal of Material Chemistry C, 6(16), 4565-4572 (2018)

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门