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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)-

2(1H)-Pyridinone, 6-chloro-, hydrazone

NNc1cccc(n1)Cl Request for Quotation
Chemical Name: 2(1H)-Pyridinone, 6-chloro-, hydrazone
CAS Number: 5193-03-3
Product Number: AG003H0L(AGN-PC-0OBMAR)
Synonyms:
MDL No:
Molecular Formula: C5H6ClN3
Molecular Weight: 143.5742

Identification/Properties

Properties
MP:
126 - 127 °C
BP:
308.6°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
143.574g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
143.025g/mol
Monoisotopic Mass:
143.025g/mol
Topological Polar Surface Area:
50.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
88.3
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

PNMR/2-CHLORO-6-HYDRAZINYLPYRIDINE-5193-03-3-hnmr.pdf

Other Analytical Data

POTHER/2-CHLORO-6-HYDRAZINYLPYRIDINE-5193-03-3-hplc.pdf

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Chemical Structure


2-Chloro-6-hydrazinopyridine, a versatile compound widely used in chemical synthesis, plays a crucial role in the development of various pharmaceuticals and agrochemicals. This compound serves as a key building block in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. Its unique structure allows for the creation of complex molecules with specific biological activities.2-Chloro-6-hydrazinopyridine is particularly valuable in the synthesis of pyrazole derivatives, which are important intermediates in organic chemistry. By reacting with different reagents and functional groups, this compound can be transformed into diverse products with varying chemical properties. Additionally, its hydrazine functional group enables it to participate in important reactions such as condensation, reduction, and nucleophilic substitution, expanding its synthetic utility.In summary, the application of 2-Chloro-6-hydrazinopyridine in chemical synthesis offers a pathway to the creation of structurally diverse compounds with potential applications in the fields of pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable tool for researchers and chemists seeking to develop novel molecules with targeted properties.