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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-chloro-6-piperazin-1-ylpyridazine;hydrochloride

Clc1ccc(nn1)N1CCNCC1.Cl Request for Quotation
Chemical Name: 3-chloro-6-piperazin-1-ylpyridazine;hydrochloride
CAS Number: 100241-11-0
Product Number: AG0001CZ(AGN-PC-0NI70U)
Synonyms:
MDL No: MFCD16620387
Molecular Formula: C8H12Cl2N4
Molecular Weight: 235.1137

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
235.112g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
234.044g/mol
Monoisotopic Mass:
234.044g/mol
Topological Polar Surface Area:
41A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
160
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


3-Chloro-6-(piperazin-1-yl)pyridazine hydrochloride, often referred to as $name$, is a versatile compound extensively used in chemical synthesis. It serves as a valuable building block in the creation of various pharmaceutical compounds, agrochemicals, and specialty chemicals. The presence of the chloro substituent on the pyridazine ring confers reactivity and specificity in various synthetic reactions. In chemical synthesis, this compound is commonly utilized as a key intermediate in the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry and drug discovery. Its piperazine functional group provides a site for structural modification, enabling the synthesis of diverse molecules with specific pharmacological properties. Furthermore, the hydrochloride salt form of 3-Chloro-6-(piperazin-1-yl)pyridazine enhances its solubility in aqueous environments, making it particularly useful in reactions that require aqueous conditions or biological applications. Overall, the application of 3-Chloro-6-(piperazin-1-yl)pyridazine hydrochloride in chemical synthesis underscores its significance as a fundamental building block for the construction of complex molecules with tailored properties and functionalities.