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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'-[(1E)-1,2-ethenediylbis(sulfonyl)]bis-

O=S(=O)(c1ccccc1)/C=C/S(=O)(=O)c1ccccc1 Request for Quotation
Chemical Name: Benzene, 1,1'-[(1E)-1,2-ethenediylbis(sulfonyl)]bis-
CAS Number: 963-16-6
Product Number: AG003UUW(AGN-PC-0OOCG4)
Synonyms:
MDL No:
Molecular Formula: C14H12O4S2
Molecular Weight: 308.3727

Identification/Properties

Properties
MP:
221-223 °C(lit.)
BP:
545°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
308.366g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
308.018g/mol
Monoisotopic Mass:
308.018g/mol
Topological Polar Surface Area:
85A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
473
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(E)-1,2-Bis(phenylsulfonyl)ethene, a versatile compound widely used in chemical synthesis, serves as a valuable building block in organic chemistry. Its ability to undergo a variety of transformations makes it highly sought after for the creation of complex organic molecules with diverse functionalities. In particular, (E)-1,2-Bis(phenylsulfonyl)ethene is commonly employed in the formation of carbon-carbon bonds through cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. Furthermore, its double bond allows for further derivatization, enabling the introduction of various substituents to tailor the compound for specific applications. This compound's utility in chemical synthesis makes it a valuable tool for organic chemists seeking efficient and practical methods for the construction of intricate molecular structures.