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176842

Sigma-Aldrich

1-Phenyl-4,5-dichloro-6-pyridazone

≥99%

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About This Item

Empirical Formula (Hill Notation):
C10H6Cl2N2O
CAS Number:
Molecular Weight:
241.07
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥99%

mp

164-166 °C (lit.)

functional group

chloro

SMILES string

ClC1=C(Cl)C(=O)N(N=C1)c2ccccc2

InChI

1S/C10H6Cl2N2O/c11-8-6-13-14(10(15)9(8)12)7-4-2-1-3-5-7/h1-6H

InChI key

VKWCOHVAHQOJGU-UHFFFAOYSA-N

Application

1-Phenyl-4,5-dichloro-6-pyridazone was used in the preparation of 1-phenyl-4-hydroxy-5-chloro-6-pyridazone[1].
The product can be used as a titrimetric reagent for thiols.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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[Effect of 2-phenyl-4,5-dichlor-3-pyridazinone upon respiration and immunoglobulin levels (author's transl)].
E Malík et al.
Bratislavske lekarske listy, 75(3), 315-321 (1981-03-01)
M L Carmellino et al.
Farmaco (Societa chimica italiana : 1989), 48(10), 1427-1438 (1993-10-01)
Some 2-sulfonyl- and 2-acylderivatives of the 4,5-dichloro-3(2H)-pyridazinone were prepared in order to test their fungicidal activity. Interesting results, both in vitro and in vivo, were obtained in particular from the alkylsulfonyl-derivatives. Genotoxic activity of 3(2H)-pyridazinones was evaluated in vitro by
Synthesis and herbicidal activity of certain 1-phenyl-6-pyridazone derivatives.
Chemical Papers, 19(5), 403-412 (1965)

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