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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)-

Methanesulfonamide, N-(2,4-dinitro-6-phenoxyphenyl)-

[O-][N+](=O)c1cc(Oc2ccccc2)c(c(c1)[N+](=O)[O-])NS(=O)(=O)C Request for Quotation
Chemical Name: Methanesulfonamide, N-(2,4-dinitro-6-phenoxyphenyl)-
CAS Number: 51765-56-1
Product Number: AG01E4MP(AGN-PC-0OBK78)
Synonyms:
MDL No:
Molecular Formula: C13H11N3O7S
Molecular Weight: 353.30734

Identification/Properties

Computed Properties
Molecular Weight:
353.305g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
4
Exact Mass:
353.032g/mol
Monoisotopic Mass:
353.032g/mol
Topological Polar Surface Area:
155A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
560
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


4',6'-Dinitro-2'-phenoxymethanesulfonanilide is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, this compound serves as an essential building block for the preparation of various pharmaceuticals, agrochemicals, and dyes. Due to the presence of nitro and phenoxymethylsulfonyl groups, 4',6'-Dinitro-2'-phenoxymethanesulfonanilide can undergo diverse chemical reactions such as nucleophilic substitution, reduction, and transition metal-catalyzed reactions. This compound finds crucial applications in the development of new drug molecules, where its structural motif plays a key role in enhancing the biological activity and pharmacokinetic profile of the final products. Furthermore, its sulfonamide moiety imparts significant polarity to the molecule, making it a valuable intermediate in the synthesis of various organic compounds with tunable solubility and physicochemical properties.