57580-64-0

Usage

Uses

Used in Pharmaceutical Synthesis:
2-FURAN-2-YL-1-METHYL-ETHYLAMINE is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a versatile building block for the development of new drugs and medications.
Used in Enzyme Inhibition Research:
In the field of biological research, 2-FURAN-2-YL-1-METHYL-ETHYLAMINE is utilized as an inhibitor of certain enzymes. Its ability to interact with specific enzymes can provide insights into enzyme function and contribute to the development of targeted therapies for various diseases.
Used in Organic Synthesis:
2-FURAN-2-YL-1-METHYL-ETHYLAMINE is also used in the production of fine chemicals and intermediates for organic synthesis. Its presence in these processes can lead to the creation of complex organic molecules with a wide range of applications.
Used in Chemical Research and Development:
In the chemical industry, 2-FURAN-2-YL-1-METHYL-ETHYLAMINE serves as a valuable compound for research and development. Its unique properties and potential applications make it an important subject for further study and innovation.

Upstream product

• 85515-92-0 1-[2]furyl-acetone oxime 
• 98-01-1 furfural 
• 134538-48-0 (E)-2-(2-nitroprop-1-en-1-yl)furan 

Relevant academic research and scientific papers

Guanidine-containing compound as well as preparation method and application thereof

The invention discloses a cyanoguanidine-containing compound as well as a preparation method and application thereof. The invention also discloses a composition containing the cyanoguanidine-structured compound (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. The invention also discloses application thereof in preparation of analgesic drugs. The compounds of the invention are useful in the treatment of various pain.

Heteroarylisopropylamines as MAO inhibitors

The in vitro monoamine oxidase inhibitory (MAOI) activities of 11 heteroarylisopropylamines vis-a-vis MAO-A and MAO-B were described and interpreted in terms of possible interactions with the enzyme active site. Molecular dynamics simulations allowed a comparison between the most active MAO-A inhibitor of the series, the 1-(2-benzofuryl)-2-aminopropane, and the specific, analogous MAO-A substrate serotonin.

Heterocyclic analogs of amphetamine: Thioureas, dithiocarbamates, and negatively substituted amides

A series of heterocyclic analogs of amphetamine was synthesized. The heterocycles employed included the 2-furyl, 2-thienyl, 3-methyl-2 thienyl, 3-pyridyl, and 6-methyl-2-pyridyl rings. The aliphatic amine group was converted to the N-methylthiourea, dithiocarbamate, methanesulfonyl, trifluoromethanesulfonyl, and trifluoroacetyl functions since similar conversions of the β-phenethylamine structure had shown blood pressure-lowering effects and some loss of behavioral effects. P-Chlorophenyl and 1-naphthyl analogs were also converted to these derivatives. Behavioral and other biological effects, including antiarthritic, passive cutaneous anaphylactic, and antimicrobial, were observed. The 3-methyl-2-thienyl analog of amphetamine significantly increased papillary muscle contractile force without producing arrhythmias.

Preparation of esters of phosphorus acids

Esters of phosphorus acids are prepared by an improved process whereby aromatic alcohols and phosphorus halides are reacted at specified temperatures in the presence of amine catalysts thereby providing high yields of substantially pure esters and allowing preparation of selected halogen-containing mono- and di-esters of phosphorus acids wherein halogen is directly bonded to phosphorus having substantially no side reactant contamination. The phosphorus esters are useful as intermediates in the preparation of plasticizers, oil additives and functional fluids.