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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-chloropyridin-2-yl)hydrazine

NNc1ncccc1Cl Request for Quotation
Chemical Name: (3-chloropyridin-2-yl)hydrazine
CAS Number: 22841-92-5
Product Number: AG003J6Z(AGN-PC-0JSTWT)
Synonyms:
MDL No: MFCD01936479
Molecular Formula: C5H6ClN3
Molecular Weight: 143.5742

Identification/Properties

Properties
MP:
165-167 °C
BP:
276.7°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
143.574g/mol
XLogP3:
1.1
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

Other Analytical Data

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Chemical Structure


3-Chloro-2-hydrazinopyridine is a versatile compound widely utilized in chemical synthesis for its unique reactivity and structural properties. In organic chemistry, it serves as a key building block in the synthesis of various heterocyclic compounds, including pyrazole derivatives. Due to its hydrazine functionality, this compound is crucial in the preparation of hydrazones and hydrazides, which are important intermediates in pharmaceutical and agrochemical industries. Additionally, 3-Chloro-2-hydrazinopyridine can participate in diverse reactions such as nucleophilic substitution, condensation, and cyclization, making it a valuable reagent for the creation of structurally complex molecules. Its role in chemical synthesis extends beyond simple transformations, offering chemists a powerful tool for developing new synthetic pathways and innovative molecular designs.