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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)-

4-Pyridazinecarbonitrile, 3-chloro-

N#Cc1ccnnc1Cl Request for Quotation
Chemical Name: 4-Pyridazinecarbonitrile, 3-chloro-
CAS Number: 1445-56-3
Product Number: AG001JND(AGN-PC-0NISL0)
Synonyms:
MDL No:
Molecular Formula: C5H2ClN3
Molecular Weight: 139.5425

Identification/Properties

Properties
BP:
362.9°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
139.542g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
138.994g/mol
Monoisotopic Mass:
138.994g/mol
Topological Polar Surface Area:
49.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
138
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-Chloropyridazine-4-carbonitrile, also known as $name$, serves as a versatile building block in chemical synthesis, particularly in the field of organic chemistry. This compound is widely utilized for its unique reactivity and ability to introduce key functionalities into complex molecular structures.One of the primary applications of 3-Chloropyridazine-4-carbonitrile is in the synthesis of biologically active molecules and pharmaceutical intermediates. Its cyano group (CN) can undergo various transformations, such as nucleophilic addition reactions, facilitating the introduction of nitrogen-containing motifs essential for drug development.Furthermore, the chlorine atom in 3-Chloropyridazine-4-carbonitrile can participate in substitution reactions, enabling the introduction of diverse substituents to tailor the properties of the final product. This versatility makes it a valuable reagent in the construction of heterocyclic compounds, which are prevalent in many natural products and pharmaceuticals.In summary, 3-Chloropyridazine-4-carbonitrile plays a crucial role in organic synthesis by providing a platform for the efficient construction of complex molecules with diverse chemical functionalities. Its applications extend to the development of new materials, agrochemicals, and pharmaceuticals, showcasing its significance in modern chemical research and innovation.