342319
3-氯-6-苯基哒嗪
98%
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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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-772-6
MDL number:
Assay:
98%
Form:
solid
InChI key
BUBRFWDEAVIFMV-UHFFFAOYSA-N
InChI
1S/C10H7ClN2/c11-10-7-6-9(12-13-10)8-4-2-1-3-5-8/h1-7H
SMILES string
Clc1ccc(nn1)-c2ccccc2
assay
98%
form
solid
mp
159-161 °C (lit.)
functional group
chloro, phenyl
General description
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.
Application
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Electrochemical carboxylation of some heteroaromatic compounds.
Fuchs P, et al.
Acta Chemica Scandinavica. Series B, 35, 185-192 (1981)
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)
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
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