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Merck
CN
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文件

680532

Sigma-Aldrich

3-(N,N-二甲氨基)苯硼酸

≥95%

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About This Item

经验公式（希尔记法）:
C8H12BNO2
CAS号:
178752-79-9
分子量:
165.00
MDL编号:
MFCD01318996
UNSPSC代码:
12352103
PubChem化学物质编号:
24885572
NACRES:
NA.22

检测方案

≥95%

mp

178-190 °C

SMILES字符串

CN(C)c1cccc(c1)B(O)O

InChI

1S/C8H12BNO2/c1-10(2)8-5-3-4-7(6-8)9(11)12/h3-6,11-12H,1-2H3

InChI key

YZQQHZXHCXAJAV-UHFFFAOYSA-N

一般描述

可含不定量的酸酐

应用

Reactant involved in synthesis of different protein effector including:
  • Modulators of survival motor neuron protein
  • Glucokinase activators
  • Aryl ethers for use as Bacillus anthracis enoyl-ACP reductase inhibitors

Reactant involved in synthesis of:
  • Thiourea-functionalized paracyclophanes
  • Low-background fluorescent imaging agents for nitric oxide

Reactant to undergo regioselective iodination and bromination

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315,H319,H335

危险分类

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

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Gözde Murat Saltan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 188, 372-381 (2017-08-02)
In an approach to develop efficient organic optoelectronic devices to be used in light-driven systems, a series of three thiophene linked benzimidazole conjugates were synthesized and characterized. The combination of two thiophene rings to a benzimidazole core decorated with different

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