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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-chloro-6-(1,1-dimethylethoxy)-

CC(Oc1ccc(nn1)Cl)(C)C Request for Quotation
Chemical Name: Pyridazine, 3-chloro-6-(1,1-dimethylethoxy)-
CAS Number: 17321-24-3
Product Number: AG001YQ4(AGN-PC-0KKPW8)
Synonyms:
MDL No:
Molecular Formula: C8H11ClN2O
Molecular Weight: 186.6387

Identification/Properties

Computed Properties
Molecular Weight:
186.639g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
186.056g/mol
Monoisotopic Mass:
186.056g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-6-(1,1-dimethylethoxy)pyridazine, a versatile compound widely utilized in chemical synthesis, serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. This unique molecule's reactive chloride group at the 3-position and the ethoxy group at the 6-position offer distinctive reactivity and selectivity profiles, making it an invaluable tool for organic chemists in the development of complex molecular structures. In addition, the presence of a pyridazine ring in its structure confers enhanced aromaticity and potential for diverse functionalization, enabling tailored modifications for specific applications. By leveraging the synthetic potential of 3-Chloro-6-(1,1-dimethylethoxy)pyridazine, chemists can efficiently access novel compounds with enhanced properties and targeted functionalities, driving innovation across various fields of chemistry and beyond.