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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)-

Benzenesulfonamide, 4-nitro-

[O-][N+](=O)c1ccc(cc1)S(=O)(=O)N Request for Quotation
Chemical Name: Benzenesulfonamide, 4-nitro-
CAS Number: 6325-93-5
Product Number: AG00365Y(AGN-PC-00BU4N)
Synonyms:
MDL No:
Molecular Formula: C6H6N2O4S
Molecular Weight: 202.1878

Identification/Properties

Properties
MP:
177-182 °C
BP:
417.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.6490 (estimate)
Computed Properties
Molecular Weight:
202.184g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
202.005g/mol
Monoisotopic Mass:
202.005g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
281
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Nitrobenzenesulfonamide is a versatile compound often utilized in chemical synthesis for its unique properties and reactivity. This compound is commonly employed as a precursor in the preparation of various pharmaceuticals and agrochemicals. Its nitro group can undergo reduction reactions to yield aromatic amines, which can further participate in coupling reactions to form complex organic molecules. Additionally, the sulfonamide functional group in 4-Nitrobenzenesulfonamide can act as a directing group in transition metal-catalyzed C-H activation reactions, enabling the selective functionalization of aromatic rings. Overall, 4-Nitrobenzenesulfonamide plays a crucial role in the construction of diverse molecular architectures in chemical synthesis.