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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-Pyridinecarboxylic acid, 2-chloro-, hydrazide

NNC(=O)c1ccnc(c1)Cl Request for Quotation
Chemical Name: 4-Pyridinecarboxylic acid, 2-chloro-, hydrazide
CAS Number: 58481-04-2
Product Number: AG00E9Y7(AGN-PC-0JOCM2)
Synonyms:
MDL No: MFCD00221428
Molecular Formula: C6H6ClN3O
Molecular Weight: 171.5843

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
171.584g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
171.02g/mol
Monoisotopic Mass:
171.02g/mol
Topological Polar Surface Area:
68A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloroisonicotinohydrazide is a versatile compound commonly utilized in chemical synthesis, particularly in the production of various pharmaceuticals and agrochemicals. This compound serves as a key building block in the creation of specialized molecules due to its unique chemical properties and reactivity.In chemical synthesis, 2-Chloroisonicotinohydrazide is often employed as a valuable intermediate in the development of novel therapeutic agents, such as anti-tuberculosis drugs and anti-cancer medications. Its ability to undergo selective reactions and form diverse chemical bonds makes it an essential component in the construction of complex organic molecules with specific pharmacological activities.Additionally, 2-Chloroisonicotinohydrazide plays a crucial role in the synthesis of biologically active compounds used in insecticides and herbicides. By incorporating this compound into the chemical structure of agrochemicals, researchers can enhance their effectiveness and specificity, ultimately leading to improved crop protection and pest control solutions.Overall, the application of 2-Chloroisonicotinohydrazide in chemical synthesis enables the efficient and strategic development of advanced pharmaceuticals and agrochemicals with targeted properties and functions. Its versatility and reliability make it a valuable tool for chemists and researchers working to address critical challenges in the fields of medicine and agriculture.