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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-Pyridinecarboxylicacid, 2-(methylthio)-, hydrazide

CSc1ncccc1C(=O)NN Request for Quotation
Chemical Name: 3-Pyridinecarboxylicacid, 2-(methylthio)-, hydrazide
CAS Number: 232926-33-9
Product Number: AG002MRY(AGN-PC-0KKNP0)
Synonyms:
MDL No:
Molecular Formula: C7H9N3OS
Molecular Weight: 183.2309

Identification/Properties

Computed Properties
Molecular Weight:
183.229g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
183.047g/mol
Monoisotopic Mass:
183.047g/mol
Topological Polar Surface Area:
93.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Methylthio)nicotinohydrazide is a versatile chemical compound widely utilized in chemical synthesis for its unique properties and applications. This compound serves as a key building block in various organic reactions, particularly in the formation of heterocyclic compounds. With its sulfur-containing methylthio group and nicotinohydrazide backbone, 2-(Methylthio)nicotinohydrazide offers a valuable platform for the development of novel molecules with potential pharmacological activities. In addition, this compound has been found to exhibit promising antimicrobial and antitumor properties, making it a valuable candidate for further research and development in drug discovery. Its ability to selectively target specific biological pathways and interactions makes it a valuable tool in medicinal chemistry and chemical biology studies. In summary, 2-(Methylthio)nicotinohydrazide plays a crucial role in advancing the field of chemical synthesis by enabling the creation of complex molecular structures with potential therapeutic applications.