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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-

O=C1CSCC1 Request for Quotation
Chemical Name: 3(2H)-Thiophenone, dihydro-
CAS Number: 1003-04-9
Product Number: AG0001HW(AGN-PC-0JL4CS)
Synonyms:
MDL No:
Molecular Formula: C4H6OS
Molecular Weight: 102.1548

Identification/Properties

Properties
BP:
175.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.528(lit.)
Computed Properties
Molecular Weight:
102.151g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
102.014g/mol
Monoisotopic Mass:
102.014g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
69.9
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tetrahydrothiophen-3-one, also known as thietane, is a versatile compound widely used in chemical synthesis. Its unique chemical structure and properties make it a valuable building block for the production of various compounds in the pharmaceutical, agrochemical, and materials industries.One of the key applications of tetrahydrothiophen-3-one in chemical synthesis is its use as a precursor in the synthesis of heterocyclic compounds. By incorporating thietane into molecular structures, chemists can introduce sulfur atoms into organic molecules, providing new avenues for the development of novel materials and bioactive compounds.Additionally, tetrahydrothiophen-3-one is commonly employed in the synthesis of sulfide-containing compounds, which have diverse applications in organic chemistry. These sulfur-containing compounds exhibit unique reactivity and properties, making them valuable intermediates in the preparation of pharmaceutical drugs, pesticides, and other fine chemicals.Overall, the utilization of tetrahydrothiophen-3-one in chemical synthesis enables the efficient construction of complex molecular architectures and the development of innovative compounds with important industrial and pharmaceutical applications.