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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)-

Glycine, N-[bis(methylthio)methylene]-, methyl ester

COC(=O)CN=C(SC)SC Request for Quotation
Chemical Name: Glycine, N-[bis(methylthio)methylene]-, methyl ester
CAS Number: 58091-08-0
Product Number: AG003SNB(AGN-PC-0LL0H3)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2S2
Molecular Weight: 193.28704

Identification/Properties

Computed Properties
Molecular Weight:
193.279g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
193.023g/mol
Monoisotopic Mass:
193.023g/mol
Topological Polar Surface Area:
89.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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


N-[Bis(methylthio)methylene]glycine methyl ester is a versatile compound that finds wide application in chemical synthesis processes. Particularly valued for its ability to serve as a key building block in the creation of complex molecules, this compound plays a crucial role in the development of various pharmaceutical, agricultural, and material science products. Its unique chemical structure enables it to engage in a range of reactions, including cycloaddition, condensation, and functional group transformations, making it an invaluable tool for organic chemists seeking to construct intricate molecular structures. Furthermore, N-[Bis(methylthio)methylene]glycine methyl ester's stability and compatibility with a diverse array of reagents and reaction conditions further enhance its utility in the synthesis of novel compounds with potential applications across a wide range of industries.