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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)-

2-Furancarboxamide, N-methoxy-N-methyl-

CON(C(=O)c1ccco1)C Request for Quotation
Chemical Name: 2-Furancarboxamide, N-methoxy-N-methyl-
CAS Number: 95091-92-2
Product Number: AG006PTN(AGN-PC-0NB4FA)
Synonyms:
MDL No:
Molecular Formula: C7H9NO3
Molecular Weight: 155.1513

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
155.153g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
155.058g/mol
Monoisotopic Mass:
155.058g/mol
Topological Polar Surface Area:
42.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Methoxy-N-methylfuran-2-carboxamide, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique properties and reactivity. This compound finds extensive applications in the field of organic chemistry, particularly in the development of pharmaceuticals, agrochemicals, and functional materials.One of the key uses of $name$ in chemical synthesis is as a protecting group for various functional groups within a molecule. By temporarily masking reactive functional groups with $name$, chemists are able to selectively carry out specific reactions without interfering with other parts of the molecule. This strategy enables the synthesis of complex organic compounds with improved efficiency and control over regioselectivity and chemoselectivity.Moreover, $name$ can also serve as a key intermediate in the preparation of heterocyclic compounds, which are prevalent in medicinal chemistry and materials science. The unique furan ring structure of $name$ can participate in various cyclization reactions, leading to the formation of diverse heterocycles with potential biological activities or electronic properties.Furthermore, the methoxy and methyl substituents on the furan ring of $name$ can be further functionalized to introduce additional molecular diversity and enhance the desired properties of the final product. This flexibility in derivatization makes $name$ a valuable tool for synthetic chemists seeking to tailor the structure and function of organic molecules for specific applications.Overall, the strategic incorporation of N-Methoxy-N-methylfuran-2-carboxamide in chemical synthesis offers a powerful approach to designing and synthesizing novel compounds with tailored properties for a wide range of industrial and scientific applications.