CAS 4753-75-7
:N-Methyl-2-furanmethanamine
Description:
N-Methyl-2-furanmethanamine, with the CAS number 4753-75-7, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. This compound features a methyl group attached to the nitrogen atom of the amine functional group, contributing to its basicity and reactivity. It is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. N-Methyl-2-furanmethanamine is known for its potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, such as nucleophilic substitutions and condensation reactions. The presence of both the furan and amine functionalities allows for diverse reactivity, making it a valuable intermediate in synthetic chemistry. Additionally, safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards.
Formula:C6H9NO
InChI:InChI=1S/C6H9NO/c1-7-5-6-3-2-4-8-6/h2-4,7H,5H2,1H3
InChI key:InChIKey=DGLIOWSKNOCHEX-UHFFFAOYSA-N
SMILES:C(NC)C1=CC=CO1
Synonyms:- (2-Furanylmethyl)methylamine
- (Furylmethyl)-methylamine
- 1-(furan-2-yl)-N-methylmethanamine
- 2-((Methylamino)methyl)furan
- 2-Furanmethanamine, N-methyl-
- Furfurylamine, N-methyl-
- Furfurylamine, N-methyl- (8CI)
- Methyl[(furan-2-yl)methyl]amine
- N-(Furan-2-ylmethyl)-N-methylamine
- N-Methyl(furan-2-ylmethyl)amine
- N-Methyl-2-furanmethanamine
- N-Methyl-N-(furan-2-ylmethyl)amine
- N-Methylfurfurylamine
- N-[(2-Furyl)methyl](methyl)amine
- Nsc 78427
- furan-2-yl-N-methylmethanaminium
- See more synonyms
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Found 4 products.
N-(2-Furylmethyl)-N-methylamine
CAS:N-(2-Furylmethyl)-N-methylaminePurity:≥95%Molecular weight:111.14g/mol1-(Furan-2-yl)-N-methylmethanamine
CAS:Formula:C6H9NOPurity:95%Color and Shape:LiquidMolecular weight:111.144(2-Furylmethyl)methylamine
CAS:<p>(2-Furylmethyl)methylamine is a protein inhibitor that has been shown to inhibit γ-secretase, an enzyme responsible for the cleavage of amyloid precursor protein (APP) and the production of beta-amyloid. It has also been shown to be effective in treating cancer and Alzheimer's disease when administered as an intravenous injection or oral medication. The effects on animals were observed in a study involving mice with bladder cancer. (2-Furylmethyl)methylamine was found to inhibit the growth of bladder cancer cells and induce apoptosis. This compound also inhibits glycogen synthase kinase 3 (GSK3), which is involved in cell proliferation. Trichophyton mentagrophytes, a fungus that causes athlete's foot, has also been found to be sensitive to this drug. Heterocycles are not affected by this compound because they lack nitrogen atoms at their positions corresponding to those in the amide group</p>Formula:C6H9NOPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:111.14 g/mol



