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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)-

Benzene, 1,1'-sulfonylbis[4-nitro-

O=S(=O)(c1ccc(cc1)[N+](=O)[O-])c1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzene, 1,1'-sulfonylbis[4-nitro-
CAS Number: 1156-50-9
Product Number: AG000G8W(AGN-PC-0JL9ZE)
Synonyms:
MDL No:
Molecular Formula: C12H8N2O6S
Molecular Weight: 308.2667

Identification/Properties

Properties
MP:
178-185°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
308.264g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
308.01g/mol
Monoisotopic Mass:
308.01g/mol
Topological Polar Surface Area:
134A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
447
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bis(4-nitrophenyl)sulfone, also known as 4,4'-dinitrodiphenyl sulfone, is a compound commonly used in chemical synthesis as a building block for various organic molecules. With its unique structure and reactivity, this sulfone compound plays a crucial role in the creation of diverse chemical reactions and functional materials.One of the key applications of Bis(4-nitrophenyl)sulfone in chemical synthesis is as a valuable precursor in the preparation of polymers, particularly in the production of high-performance engineering plastics such as poly(aryl ethersulfone) and poly(aryl ethersulfone ketone). These polymers exhibit exceptional thermal and chemical resistance, making them ideal for use in demanding industrial applications where stability and durability are essential.Furthermore, Bis(4-nitrophenyl)sulfone is widely utilized as a reagent in the synthesis of pharmaceutical intermediates and fine chemicals. Its ability to undergo nucleophilic substitution reactions allows for the creation of complex molecular structures with precise control over stereochemistry and functional group placement, making it a versatile tool in organic chemistry research and drug discovery.Overall, Bis(4-nitrophenyl)sulfone's versatility and reactivity make it a valuable component in the toolkit of synthetic chemists, enabling the synthesis of a wide range of functional materials and organic compounds with diverse applications in industry and academia.