6788-68-7

Basic information

• Product Name: 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE
• Synonyms: BUTTPARK 95\04-14;3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE;3-[(Fur-2-ylmethyl)amino]propanenitrile;3-(FURFURYLAMINO)PROPIONITRILE
• CAS NO: 6788-68-7
• Molecular Formula: C₈H₁₀N₂O
• Molecular Weight: 150.18
• Product Categories: Furans, Benzofurans & Dihydrobenzofurans;Furans, Benzofurans & Dihydrobenzofurans
• Mol File: 6788-68-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 142 °C
• Appearance: /
• CAS DataBase Reference: 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE(6788-68-7)
• EPA Substance Registry System: 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE(6788-68-7)

Safety Data

• Hazard Codes: C,Xi,Xn
• Statements: 22
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S36/37/39:Wear suitabl
• HazardClass: IRRITANT
• Hazardous Substances Data: 6788-68-7(Hazardous Substances Data)

Usage

Description

3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE is a chemical compound with the molecular formula C9H10N2O. It is an organic compound that contains a furan ring substituted with an amino group and a nitrile group. This versatile compound is known for its reactivity and wide range of applications, making it a valuable intermediate in various chemical processes.

Uses

Used in Pharmaceutical Industry:
3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE serves as an intermediate in the production of agrochemicals, aiding in the creation of substances that can enhance crop protection and yield.
Used in Dye Production:
3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE is used as a chemical intermediate for the production of dyes, where its unique structure allows for the creation of a variety of colorants for different applications.
Used in Flavor and Fragrance Industry:
3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE is also utilized in the flavor and fragrance industry, where it acts as a building block for creating unique scents and tastes in various consumer products.
Safety Note:
It is important to handle and store 3-[(2-FURYLMETHYL)AMINO]PROPANENITRILE with caution due to its potential toxicity and health hazards, ensuring that proper safety measures are in place during its use and disposal.

Upstream product

• 617-89-0 furan-2-ylmethanamine 
• 107-13-1 acrylonitrile 
• 2417-90-5 bromopropionitrile 

Relevant articles and documents

A Combined Experimental–Theoretical Study on Diels-Alder Reaction with Bio-Based Furfural: Towards Renewable Aromatics

The synthesis of relevant renewable aromatics from bio-based furfural derivatives and cheap alkenes is carried out by using a Diels-Alder/aromatization sequence. The prediction and the control of the ortho/meta selectivity in the Diels-Alder step is an important issue to pave the way to a wide range of renewable aromatics, but it remains a challenging task. A combined experimental-theoretical approach reveals that, as a general trend, ortho and meta cycloadducts are the kinetic and thermodynamic products, respectively. The nature of substituents, both on the dienes and dienophiles, significantly impacts the feasibility of the reaction, through a modulation on the nucleo- and electrophilicity of the reagents, as well as the ortho/meta ratio. We show that the ortho/meta selectivity at the reaction equilibrium stems from a subtle interplay between charge interactions, favoring the ortho products, and steric interactions, favoring the meta isomers. This work also points towards a path to optimize the aromatization step.

Probing Carbocatalytic Activity of Carbon Nanodots for the Synthesis of Biologically Active Dihydro/Spiro/Glyco Quinazolinones and Aza-Michael Adducts

Herein, we report the fluorescent carbon dots as an effective and recyclable carbocatalyst for the generation of carbon-heteroatom bond leading to quinazolinone derivatives and aza-Michael adducts under mild reaction conditions. The results establish this nanoscale form of carbon as an alternative carbocatalyst for important acid catalyzed organic transformations. The mild surface acidity of carbon dots imparted by -COOH functionality could effectively catalyze the formation of synthetically challenging spiro/glycoquinazolinones under the present reaction conditions.