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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-(methylsulfonyl)-

OC(=O)CNS(=O)(=O)C Request for Quotation
Chemical Name: Glycine, N-(methylsulfonyl)-
CAS Number: 35688-18-7
Product Number: AG003SER(AGN-PC-0KPVQH)
Synonyms:
MDL No: MFCD00069044
Molecular Formula: C3H7NO4S
Molecular Weight: 153.1570

Identification/Properties

Properties
BP:
344.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
153.152g/mol
XLogP3:
-1.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
153.01g/mol
Monoisotopic Mass:
153.01g/mol
Topological Polar Surface Area:
91.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
188
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
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

PNMR/N-METHYLSULFONYLGLYCINE-35688-18-7-hnmr.pdf

Other Analytical Data

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Chemical Structure


N-(Methylsulfonyl)glycine, also known as DMG, is a versatile compound utilized in chemical synthesis for its ability to act as a methyl donor. Its unique structure contains a sulfur atom attached to a methyl group and a glycine molecule, making it a valuable intermediate in various chemical reactions. In chemical synthesis, DMG is often employed as a source of methyl groups for methylation reactions, playing a crucial role in the modification of organic compounds. Additionally, DMG can participate in the formation of complex molecules through its methyl transfer capabilities, enabling the creation of a wide range of functionalized products. Its application in chemical synthesis extends to pharmaceuticals, polymers, and materials science, where precise control over methylation reactions is essential for developing new compounds with desired properties.