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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-(acetylamino)-N-methyl-

COS(=O)(=O)[O-].COc1ccc2c(c1)oc(n2)c1n(C)c2c([n+]1C)cccc2 Request for Quotation
Chemical Name: Acetamide, 2-(acetylamino)-N-methyl-
CAS Number: 7606-79-3
Product Number: AG005SBS(AGN-PC-0JRABR)
Synonyms:
MDL No:
Molecular Formula: C18H19N3O6S
Molecular Weight: 405.4250

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
130.147g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
130.074g/mol
Monoisotopic Mass:
130.074g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
122
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


2-Acetamido-N-methylacetamide, also known as N-acetyl-N-methylglycine, is a versatile compound widely used in chemical synthesis for its unique properties. In organic chemistry, it serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its functionality as a modified amino acid derivative allows for the formation of complex molecular structures with enhanced biological activities. Additionally, 2-Acetamido-N-methylacetamide is utilized in the development of novel materials such as polymers and biomaterials due to its ability to contribute to specific chemical reactions and structural motifs. Its application in chemical synthesis extends to the fields of medicinal chemistry, materials science, and organic synthesis, where its versatility and reactivity play a crucial role in the design and production of innovative compounds with tailored properties.