14261-92-8

Usage

Molecular structure

The compound has an isoindole ring, a carboxylic acid group, and a phenyl group.

Physical form

It is a white to off-white solid.

Usage

The compound is used in research and development activities in the pharmaceutical and chemical industries.

Potential applications

It has potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique molecular structure and reactivity.

Safety

It is important to handle this chemical with care and follow proper safety protocols when working with it in a laboratory setting.

Upstream product

• 62-53-3 aniline 
• 3237-23-8 N-(2-furylmethylene)aniline 
• 4439-56-9 N-(furan-2-ylmethyl)aniline 

Relevant academic research and scientific papers

SMALL MOLECULE INHIBITORS OF APOBEC3G AND APOBEC3B

The present invention is directed to compositions and methods for inhibition of APOBEC-related DNA cytosine deaminase enzymes, and to methods of using the compounds for treatment of a disease in a patient, such as an infectious disease or a cancer. The in

Cycloaddition of furfurylamines to maleic anhydride and its substituted derivatives

The regio- and stereoselectivity of the [4+2] cycloaddition of maleic, citraconic, dichloromaleic, and dibromomaleic anhydrides to difurfuryl amines and secondary furfurylamines were studied. N-Furfuryl-, N-phenyl-, and N-benzylhexahydrooxoepoxyisoindole-7-carboxylic acids were synthesized. An approach was developed for obtaining hexahydroepoxyoxoisoindole-7-carboxylic acid unsubstituted at the nitrogen atom. Aromatization of the oxabicycloheptene fragment of the dihaloepoxyiso-indolonecarboxylic acids gave a series of 7-carboxy-2-R-isoindol-1-ones.

Preparative synthesis of 7-carboxy-2-R-isoindol-1-ones

A preparative method for the synthesis of 7-carboxy-2-R-isoindol-1-ones was developed on the basis of the [4+2] cycloaddition of secondary furfurylamines to maleic anhydride.