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Home  > [3-(2-Furyl)phenyl]amine HCl

AA08985

102269-42-1 | [3-(2-Furyl)phenyl]amine HCl

Packsize Purity Availability Price Discounted Price    Quantity
500mg 95% 2 weeks $667.00 $467.00 -   +
1g 95% 2 weeks $727.00 $509.00 -   +
5g 95% 2 weeks $1,421.00 $995.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA08985
Chemical Name: [3-(2-Furyl)phenyl]amine HCl
CAS Number: 102269-42-1
Molecular Formula: C10H9NO
Molecular Weight: 159.1846
MDL Number: MFCD04039071
SMILES: Nc1cccc(c1)c1ccco1

 

Upstream Synthesis Route
  • 3-(Furan-2-yl)aniline, also known as furan-2-ylphenylamine, is a versatile compound widely used in chemical synthesis. Its unique structure, combining a furan ring with an aniline group, provides numerous opportunities for the creation of various functional molecules.In chemical synthesis, 3-(Furan-2-yl)aniline serves as a valuable building block for the preparation of diverse heterocyclic compounds. The furan ring imparts aromaticity and electron density, while the aniline moiety offers reactivity and functional group compatibility. This compound is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its ability to introduce both furan and aniline functionalities into target molecules.One notable application of 3-(Furan-2-yl)aniline is in the synthesis of biologically active compounds. By incorporating this versatile building block into the structure of drug candidates, researchers can modulate the pharmacological properties and enhance the potency of the resulting molecules. Additionally, the presence of both furan and aniline groups in the final product can facilitate further derivatization and structural modifications to fine-tune the desired biological activities.Moreover, 3-(Furan-2-yl)aniline is utilized in the preparation of functional materials with specific properties. The presence of the furan ring can confer desirable electronic properties, such as π-conjugation and electron delocalization, making the resulting materials suitable for applications in organic electronics, optoelectronics, and catalysis. By incorporating this compound into the design of polymers, ligands, or small molecules, chemists can tailor the material properties to meet the requirements of various technological applications.
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