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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)-

Benzamide, N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propenyl]-

ONC(=O)C=Cc1cccc(c1)C(=O)NO Request for Quotation
Chemical Name: Benzamide, N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propenyl]-
CAS Number: 174664-65-4
Product Number: AG001ZUQ(AGN-PC-0JK6AS)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O4
Molecular Weight: 222.1974

Identification/Properties

Computed Properties
Molecular Weight:
222.2g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
222.064g/mol
Monoisotopic Mass:
222.064g/mol
Topological Polar Surface Area:
98.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
291
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
1
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzamide, N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propen-1-yl]- is a versatile chemical compound commonly used in chemical synthesis processes. This compound serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of functional groups, making it a valuable building block in organic synthesis.In chemical synthesis, Benzamide, N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propen-1-yl]- is employed as a reagent for the formation of heterocycles and other complex organic molecules. Its reactive hydroxyamino and oxo-propenyl groups enable the selective modification of target molecules, facilitating the creation of new compounds with desired properties. Furthermore, this compound can participate in various transformation reactions, such as acylation, condensation, and cyclization, offering a wide range of synthetic possibilities.Overall, Benzamide, N-hydroxy-3-[3-(hydroxyamino)-3-oxo-1-propen-1-yl]- plays a crucial role in advancing the field of chemical synthesis by providing synthetic chemists with a powerful tool for the efficient and precise construction of diverse chemical structures.