110677-54-8

Usage

Uses

Used in Pharmaceutical Industry:
6-BENZOFURANAMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its unique structure and reactivity to contribute to the development of new drugs.
Used in Dye Industry:
In the dye industry, 6-BENZOFURANAMINE is utilized as an intermediate in the production of dyes, taking advantage of its chemical properties to create a range of colorants for different applications.
Used in Research and Development:
6-BENZOFURANAMINE is employed in research settings for studying its potential biological activity and exploring its use in treating various medical conditions, contributing to the advancement of medical science and drug discovery.

Upstream product

• 57786-33-1 6-nitrobenzofuran 
• 57786-34-2 6-amino-2,3-dihydrobenzofuran 
• 64209-68-3 6-nitro-1-benzofuran-2-carboxylic acid 
• 69603-99-2 6-nitrobenzofuran-2-carboxylic acid ethyl ester 
• 2460-58-4 2-hydroxy-4-nitrobenzaldehyde 
• 7168-85-6 7-methoxybenzofuran 
• 4790-81-2 benzofuran-7-ol 

Downstream Products

• 57786-34-2 6-amino-2,3-dihydrobenzofuran 

Relevant academic research and scientific papers

SARS-COV-2 INHIBITORS HAVING COVALENT MODIFICATIONS FOR TREATING CORONAVIRUS INFECTIONS

Provided herein are compounds, pharmaceutical compositions and methods for treating a SARS-CoV-2 infection.

One-Pot Generation of Benzynes from Phenols: Formation of Primary Anilines by the Deoxyamination of Phenols

Benzynes were selectively generated in situ from phenols and trapped regioselectively with potassium hexamethyldisilazide to form primary anilines following acidic workup. The direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the preparation of primary aryl amines that are hard to synthesize by using coupling reactions involving phenol derivatives with ammonia. Whereas reactions of ortho- and meta-substituted phenols produced meta-substituted anilines exclusively, those of para-substituted phenols provided ortho-silylanilines.

SUBSTITUTED TRIAZOLE DERIVATIVES AS OXYTOCIN ANTAGONISTS

The present invention relates to a class of substituted triazoles of formula (I) with activity as oxytocin antagonists, uses thereof, processes for the preparation thereof and compositions containing said inhibitors. These inhibitors have utility in a variety of therapeutic areas including sexual dysfunction, particularly premature ejaculation (P.E.).

1,3-Disubstituted benzazepines as novel, potent, selective neuropeptide Y Y1 receptor antagonists

A novel series of potent and selective non-peptide neuropeptide Y (NPY) Y1 receptor antagonists, having benzazepine nuclei, have been designed, synthesized, and evaluated for activity. Chemical modification of the R1 and R3 substitue