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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)-

3(2H)-Thiophenone, dihydro-4-methyl-

O=C1CSCC1C Request for Quotation
Chemical Name: 3(2H)-Thiophenone, dihydro-4-methyl-
CAS Number: 50565-25-8
Product Number: AG006XV8(AGN-PC-0OBDDB)
Synonyms:
MDL No:
Molecular Formula: C5H8OS
Molecular Weight: 116.1814

Identification/Properties

Computed Properties
Molecular Weight:
116.178g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
116.03g/mol
Monoisotopic Mass:
116.03g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
90.1
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methyldihydrothiophen-3(2H)-one, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique reactivity and properties. In organic chemistry, $name$ serves as a valuable building block in the synthesis of various functionalized molecules and heterocyclic compounds.One key application of 4-Methyldihydrothiophen-3(2H)-one is its role as a precursor in the preparation of thioether derivatives. By reacting $name$ with different electrophiles or nucleophiles, chemists can introduce specific functional groups or substituents onto the sulfur atom of the thiophene ring. This enables the synthesis of diverse thioether-containing molecules with tailored properties for pharmaceutical, agrochemical, and material science applications.Furthermore, 4-Methyldihydrothiophen-3(2H)-one can undergo various synthetic transformations such as oxidation, reduction, and condensation reactions to yield structurally complex compounds. Its presence in the synthesis of sulfur-containing compounds contributes to the development of new drug candidates, fragrances, and polymers with enhanced chemical and biological activities.In summary, the strategic use of 4-Methyldihydrothiophen-3(2H)-one in chemical synthesis allows for the creation of diverse molecular architectures with valuable applications across different industries.