跳转至内容
Merck
CN

342319

Sigma-Aldrich

3-氯-6-苯基哒嗪

98%

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C10H7ClN2
化学文摘社编号:
分子量:
190.63
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

方案

98%

表单

solid

mp

159-161 °C (lit.)

官能团

chloro
phenyl

SMILES字符串

Clc1ccc(nn1)-c2ccccc2

InChI

1S/C10H7ClN2/c11-10-7-6-9(12-13-10)8-4-2-1-3-5-8/h1-7H

InChI key

BUBRFWDEAVIFMV-UHFFFAOYSA-N

一般描述

3-Chloro-6-phenylpyridazine is an heteroaromatic compound and is investigated by cyclic voltammetry and preparative scale electrolysis in the presence and absence of carbon dioxide. Fluorination of 3-chloro-6-phenylpyridazine with KF under solvent-free conditions in the presence of a phase transfer agent, with or without microwave irradiation is reported.

应用

3-Chloro-6-phenylpyridazine may be used in the synthesis of 6-substituted phenyl-2-(3í-substituted phenylpyridazin-6í-yl)-2,3,4,5-tetrahydropyridazin-3-ones.

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

储存分类代码

11 - Combustible Solids

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

法规信息

新产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

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

Electrochemical carboxylation of some heteroaromatic compounds.
Fuchs P, et al.
Acta Chemica Scandinavica. Series B, 35, 185-192 (1981)
Mojahidul Islam et al.
Acta poloniae pharmaceutica, 65(3), 353-362 (2008-07-24)
A series of 6-substituted phenyl-2-(3'-substituted phenyl pyridazin-6'-yl)-2,3,4,5-tetrahydropyridazin-3-ones has been synthesized. An appropriate aromatic hydrocarbon reacts with succinic anhydride in presence of AlCl3 to yield beta-aroyl propionic acid. The corresponding acid was cyclized with hydrazine hydrate to give 6-(substituted aryl)-2,3,4,5-tetrahydro-3-pyridazinone, which
Selective and efficient fluorination of chlorodiazines under solvent-free phase transfer catalysis.
Marque S, et al.
Journal of Fluorine Chemistry, 125(12), 1847-1851 (2004)

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.

联系客户支持