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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)-

methyl 3-(2,2-dimethylbutanoylsulfanyl)propanoate

COC(=O)CCSC(=O)C(CC)(C)C Request for Quotation
Chemical Name: methyl 3-(2,2-dimethylbutanoylsulfanyl)propanoate
CAS Number: 938063-63-9
Product Number: AG00IHUY(AGN-PC-0736M7)
Synonyms:
MDL No:
Molecular Formula: C10H18O3S
Molecular Weight: 218.3131

Identification/Properties

Computed Properties
Molecular Weight:
218.311g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
218.098g/mol
Monoisotopic Mass:
218.098g/mol
Topological Polar Surface Area:
68.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
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


Methyl 3-[(2,2-dimethyl-1-oxobutyl)thio]propanoate, also known as $name$, is a valuable compound in chemical synthesis. This compound is commonly used as a versatile building block for the creation of various organic molecules. In chemical synthesis, $name$ can serve as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, fragrances, and other fine chemicals.Due to its unique structure, $name$ can participate in a variety of reaction pathways, allowing chemists to functionalize it further to create more complex molecules. Its thioester functionality makes it a useful substrate for thiol-ene reactions, thiol-Michael additions, and other sulfur-mediated transformations. Additionally, the presence of the ester group can enable easy modification through esterification or transesterification reactions.In summary, the application of Methyl 3-[(2,2-dimethyl-1-oxobutyl)thio]propanoate in chemical synthesis lies in its role as a versatile and flexible building block for the efficient construction of diverse organic compounds with potential applications in various industries.