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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-methoxy-

COc1cccnn1 Request for Quotation
Chemical Name: Pyridazine, 3-methoxy-
CAS Number: 19064-65-4
Product Number: AG002EOW(AGN-PC-0JPCP9)
Synonyms:
MDL No:
Molecular Formula: C5H6N2O
Molecular Weight: 110.1139

Identification/Properties

Computed Properties
Molecular Weight:
110.116g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
110.048g/mol
Monoisotopic Mass:
110.048g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
67.4
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


Pyridazine, 3-methoxy- is a versatile compound that finds wide applications in chemical synthesis. This particular derivative of pyridazine is commonly utilized as a building block in the development of various pharmaceuticals, agrochemicals, and materials. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules. Researchers and chemists often use Pyridazine, 3-methoxy- as a key starting material in the preparation of nitrogen-containing heterocycles and other biologically active compounds. Its presence in the chemical toolbox enables the creation of novel compounds with diverse properties and functionalities, furthering the advancement of science and technology.