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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)-

3-Pyridinecarboxamide, N-methoxy-N-methyl-

CON(C(=O)c1cccnc1)C Request for Quotation
Chemical Name: 3-Pyridinecarboxamide, N-methoxy-N-methyl-
CAS Number: 95091-91-1
Product Number: AG00IIQD(AGN-PC-0N6KG7)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
161
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Methoxy-N-methylnicotinamide, commonly referred to as MMNA, is a versatile compound used in various chemical synthesis applications. This compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.In chemical synthesis, MMNA functions as a functional group manipulator, allowing chemists to introduce specific functionalities or stereochemical features into target molecules. Its methoxy and methyl substituents can be selectively modified or removed under controlled conditions, enabling precise modifications in the synthesis of complex organic compounds.Furthermore, MMNA acts as a protecting group for nitrogen-containing functionalities, providing temporary shielding during chemical reactions to prevent unwanted side reactions or undesired interactions. This protective role facilitates the efficient synthesis of intricate molecular structures by safeguarding sensitive functional groups until the desired modifications are complete.Overall, the application of N-Methoxy-N-methylnicotinamide in chemical synthesis offers chemists a strategic tool for the smooth and controlled construction of diverse organic molecules with tailored properties and functionalities.