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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)-

Furan, 2,2'-[thiobis(methylene)]bis-

S(Cc1ccco1)Cc1ccco1 Request for Quotation
Chemical Name: Furan, 2,2'-[thiobis(methylene)]bis-
CAS Number: 13678-67-6
Product Number: AG0012CV(AGN-PC-0JL4LT)
Synonyms:
MDL No: MFCD00010081
Molecular Formula: C10H10O2S
Molecular Weight: 194.2502

Identification/Properties

Properties
MP:
29-34°C
BP:
269.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.248g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
194.04g/mol
Monoisotopic Mass:
194.04g/mol
Topological Polar Surface Area:
51.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
136
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bis(furan-2-ylmethyl)sulfane, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and materials. In chemical synthesis, $name$ can act as a catalyst, a stabilizer, or a precursor, depending on the specific reaction conditions and desired end products.One key application of Bis(furan-2-ylmethyl)sulfane in chemical synthesis is its role as a cross-coupling reagent in the formation of carbon-carbon bonds. This compound can facilitate the coupling of aromatic and heteroaromatic substrates, leading to the synthesis of complex organic compounds with important applications in pharmaceuticals, agrochemicals, and materials science. Additionally, $name$ can be employed in the construction of functionalized molecules through various reactions such as carbonylation, arylation, and nucleophilic substitution.Furthermore, Bis(furan-2-ylmethyl)sulfane exhibits excellent stability and compatibility with a wide range of functional groups, making it a valuable tool for chemists working in the field of synthetic organic chemistry. Its high reactivity and selectivity enable efficient and controlled transformations, allowing for the synthesis of intricate molecular architectures with high yields and purity.Overall, Bis(furan-2-ylmethyl)sulfane plays a crucial role in advancing chemical synthesis processes by enabling the efficient construction of complex organic molecules with diverse functionalities and applications. Its versatility and reliability make it an indispensable reagent for chemists seeking to explore new synthetic pathways and develop novel compounds for various industries.