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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-acetylhydrazide

O=C(c1ccncc1)NNC(=O)C Request for Quotation
Chemical Name: 4-Pyridinecarboxylic acid, 2-acetylhydrazide
CAS Number: 1078-38-2
Product Number: AG007VKT(AGN-PC-0JLAC7)
Synonyms:
MDL No:
Molecular Formula: C8H9N3O2
Molecular Weight: 179.1760

Identification/Properties

Computed Properties
Molecular Weight:
179.179g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
179.069g/mol
Monoisotopic Mass:
179.069g/mol
Topological Polar Surface Area:
71.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
200
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-Acetylisonicotinohydrazide, also known as isonicotinoyl hydrazide, is a versatile chemical compound commonly used in chemical synthesis. This compound is widely utilized as a key building block in the preparation of various pharmaceuticals and agrochemicals. Its unique structure and properties make it an essential intermediate in the synthesis of biologically active compounds.In chemical synthesis, 2-Acetylisonicotinohydrazide serves as a crucial starting material for the production of diverse heterocyclic compounds. Its hydrazide functional group allows for the formation of hydrazones, which are important intermediates in many organic reactions. Additionally, the acetyl group on the molecule can be easily modified to introduce different substituents, enabling the synthesis of a wide range of derivatives with tailored properties.This compound is particularly valued in medicinal chemistry for its potential applications in developing new drugs. 2-Acetylisonicotinohydrazide derivatives have exhibited various biological activities, including antimicrobial, antitumor, and anti-inflammatory properties. Researchers harness the versatile reactivity of this compound to design and synthesize novel molecules with enhanced pharmacological profiles.Moreover, 2-Acetylisonicotinohydrazide plays a significant role in the synthesis of herbicides, insecticides, and other agricultural chemicals. Its structural versatility and reactivity make it a valuable tool for creating target-specific agrochemicals with improved efficacy and environmental safety.Overall, the diverse applications of 2-Acetylisonicotinohydrazide in chemical synthesis underscore its importance as a key component in the development of pharmaceuticals and agrochemicals. Researchers and chemists leverage its unique properties to advance innovation in drug discovery and crop protection, ultimately contributing to the enhancement of human health and agricultural sustainability.