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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)-

Ethyl phenyl sulfoxide

CCS(=O)c1ccccc1 Request for Quotation
Chemical Name: Ethyl phenyl sulfoxide
CAS Number: 4170-80-3
Product Number: AG0075IP(AGN-PC-0WAKIR)
Synonyms:
MDL No:
Molecular Formula: C8H10OS
Molecular Weight: 154.2294

Identification/Properties

Computed Properties
Molecular Weight:
154.227g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
154.045g/mol
Monoisotopic Mass:
154.045g/mol
Topological Polar Surface Area:
36.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
116
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


(Ethylsulfinyl)benzene, also known as ethyl phenyl sulfoxide, is a versatile compound widely used in chemical synthesis. One of its key applications is as a chiral auxiliary in asymmetric synthesis. By utilizing (Ethylsulfinyl)benzene, chemists are able to control the stereochemistry of reactions, leading to the formation of specific enantiomers with high levels of selectivity. This compound has been particularly valuable in the synthesis of pharmaceuticals and agrochemicals where enantiomeric purity is crucial for their effectiveness and safety. Additionally, (Ethylsulfinyl)benzene can serve as a precursor for the preparation of various sulfoxide derivatives through functional group transformations, expanding its utility in organic synthesis. Its compatibility with a wide range of reagents and reaction conditions makes (Ethylsulfinyl)benzene a valuable tool for chemists seeking to streamline their synthesis strategies and access complex molecular structures efficiently.