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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3(2H)-Pyridazinone, 4,5-dichloro-2-phenyl-

Clc1cnn(c(=O)c1Cl)c1ccccc1 Request for Quotation
Chemical Name: 3(2H)-Pyridazinone, 4,5-dichloro-2-phenyl-
CAS Number: 1698-53-9
Product Number: AG007UL1(AGN-PC-0JLATE)
Synonyms:
MDL No:
Molecular Formula: C10H6Cl2N2O
Molecular Weight: 241.0734

Identification/Properties

Computed Properties
Molecular Weight:
241.071g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
239.986g/mol
Monoisotopic Mass:
239.986g/mol
Topological Polar Surface Area:
32.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
332
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dichloro-2-phenylpyridazin-3(2H)-one is a highly versatile compound widely used in chemical synthesis processes. Its unique structure allows it to act as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In organic chemistry, this compound serves as an important intermediate for the synthesis of diverse heterocyclic compounds with potent biological activities. Its ability to undergo diverse chemical reactions makes it an essential tool in the development of novel compounds with potential therapeutic applications.