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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)-

Benzenemethanesulfonamide, 4-nitro-

[O-][N+](=O)c1ccc(cc1)CS(=O)(=O)N Request for Quotation
Chemical Name: Benzenemethanesulfonamide, 4-nitro-
CAS Number: 88918-72-3
Product Number: AG00494K(AGN-PC-0KKKDS)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O4S
Molecular Weight: 216.2144

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
216.211g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
216.02g/mol
Monoisotopic Mass:
216.02g/mol
Topological Polar Surface Area:
114A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
295
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


The (4-Nitrophenyl)methanesulfonamide compound plays a crucial role in chemical synthesis as a versatile building block with multiple applications. Known for its stability and reactivity, this compound is commonly used in organic chemistry reactions to introduce the phenylsulfonamide group into various molecular structures. By strategically incorporating (4-Nitrophenyl)methanesulfonamide, chemists can modify functional groups, enhance biological activity, and improve the overall properties of the target molecules. Whether employed in pharmaceutical research, material science, or agrochemical development, this compound's unique properties make it a valuable tool for creating novel compounds with diverse applications.