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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)-

Octanediamide, N-hydroxy-N'-3-pyridinyl-

ONC(=O)CCCCCCC(=O)Nc1cccnc1 Request for Quotation
Chemical Name: Octanediamide, N-hydroxy-N'-3-pyridinyl-
CAS Number: 382180-17-8
Product Number: AG003U33(AGN-PC-0JK739)
Synonyms:
MDL No:
Molecular Formula: C13H19N3O3
Molecular Weight: 265.3083

Identification/Properties

Properties
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Solubility:
DMSO: soluble10mg/mL (clear solution)
Computed Properties
Molecular Weight:
265.313g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
265.143g/mol
Monoisotopic Mass:
265.143g/mol
Topological Polar Surface Area:
91.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
284
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


Pyroxamide, a powerful reagent in chemical synthesis, has gained significant recognition for its versatile applications. Its unique properties make it an essential tool for organic chemists striving for efficient and precise reactions.One of the key applications of Pyroxamide lies in its ability to act as a reagent in the formation of amide bonds. This process, known as amide bond formation, is crucial in the creation of various pharmaceuticals, agrochemicals, and other complex organic compounds. Pyroxamide's efficiency in facilitating this reaction makes it a valuable asset in drug discovery and development.Furthermore, Pyroxamide's versatility extends to its role as a catalyst in synthetic transformations. Its ability to accelerate reactions, such as carbon-carbon bond formations or cyclizations, enables chemists to streamline their processes and achieve high yields of desired products in a shorter time frame. This is especially beneficial in the development of new materials or the synthesis of natural products.Overall, Pyroxamide's diverse applications in chemical synthesis make it a valuable and indispensable tool for researchers and chemists striving to push the boundaries of organic chemistry and achieve innovative discoveries.