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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)-

Pyridazine, 3,6-dichloro-4,5-dimethyl-

Cc1c(Cl)nnc(c1C)Cl Request for Quotation
Chemical Name: Pyridazine, 3,6-dichloro-4,5-dimethyl-
CAS Number: 34584-69-5
Product Number: AG0033JY(AGN-PC-037ALE)
Synonyms:
MDL No: MFCD00067745
Molecular Formula: C6H6Cl2N2
Molecular Weight: 177.0312

Identification/Properties

Properties
BP:
317.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
177.028g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
175.991g/mol
Monoisotopic Mass:
175.991g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3,6-Dichloro-4,5-dimethylpyridazine serves as a key building block in chemical synthesis processes. With its distinct chemical structure, it finds versatile applications in the creation of various advanced materials and pharmaceutical intermediates. Its unique reactivity allows for precise control over the formation of intricate molecular structures, making it an invaluable component in the development of new organic compounds. Through strategic incorporation into synthetic pathways, 3,6-Dichloro-4,5-dimethylpyridazine plays a crucial role in the synthesis of complex molecules with diverse functionalities, contributing significantly to the advancement of modern chemical research and industrial production processes.