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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)-

Acetamide, 2-chloro-N-(tetrahydro-2-oxo-3-thienyl)-

ClCC(=O)NC1CCSC1=O Request for Quotation
Chemical Name: Acetamide, 2-chloro-N-(tetrahydro-2-oxo-3-thienyl)-
CAS Number: 84611-22-3
Product Number: AG00G24X(AGN-PC-0LU9G9)
Synonyms:
MDL No:
Molecular Formula: C6H8ClNO2S
Molecular Weight: 193.6512

Identification/Properties

Computed Properties
Molecular Weight:
193.645g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
192.996g/mol
Monoisotopic Mass:
192.996g/mol
Topological Polar Surface Area:
71.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
185
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Chloro-N-(2-oxotetrahydrothiophen-3-yl)acetamide is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural characteristics. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. In organic synthesis, it acts as a valuable intermediate for the preparation of a wide range of heterocyclic compounds through different reaction pathways, such as acylation, substitution, or condensation reactions. Additionally, the presence of the chlorine atom and the ketone group in its structure provides opportunities for further derivatization, enabling the introduction of various functional groups to tailor the properties of the final products. Its use in chemical synthesis extends to the creation of complex molecules with specific biological activities or material properties, making it a valuable tool for synthetic chemists in the research and development of novel compounds.