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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'-sulfinylbis[4-chloro-

Clc1ccc(cc1)S(=O)c1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzene, 1,1'-sulfinylbis[4-chloro-
CAS Number: 3085-42-5
Product Number: AG0031I6(AGN-PC-0JKE0L)
Synonyms:
MDL No:
Molecular Formula: C12H8Cl2OS
Molecular Weight: 271.1623

Identification/Properties

Properties
MP:
141-144 °C(lit.)
BP:
406.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
271.155g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
269.967g/mol
Monoisotopic Mass:
269.967g/mol
Topological Polar Surface Area:
36.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
219
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:
H302-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


4,4'-Sulfinylbis(chlorobenzene), also known as bis(4-chlorophenyl)sulfone, is a versatile compound widely used in chemical synthesis. Its application in organic chemistry extends to various reactions and processes, making it a valuable reagent for synthesizing a range of compounds.In chemical synthesis, 4,4'-Sulfinylbis(chlorobenzene) serves as a key building block for creating complex structures in organic molecules. It participates in reactions such as cross-coupling, oxidative coupling, and nucleophilic substitution, allowing chemists to access diverse functional groups and frameworks.One notable application of 4,4'-Sulfinylbis(chlorobenzene) is its role in the synthesis of biaryl sulfones, which are important structural motifs found in pharmaceuticals, agrochemicals, and materials science. By utilizing this compound, chemists can introduce sulfur-containing linkages into molecules, enhancing their properties and potential applications.Furthermore, 4,4'-Sulfinylbis(chlorobenzene) can be employed in the preparation of polyphenylene sulfide (PPS) polymers, which have excellent thermal and chemical resistance. Its ability to link aromatic rings through the sulfur-containing sulfinyl group enables the formation of strong and heat-resistant polymer chains, making it valuable in high-performance material synthesis.Overall, the versatility of 4,4'-Sulfinylbis(chlorobenzene) in chemical synthesis opens up opportunities for creating new molecules with diverse functionalities and applications. Its strategic use in organic transformations contributes to the development of advanced materials, pharmaceuticals, and specialized chemicals.