7065-05-6

Basic information

• Product Name: 2-(but-3-en-2-yl)isoindoline-1,3-dione
• Synonyms: 2-(but-3-en-2-yl)isoindoline-1,3-dione;2-(1-methyl-2-propen-1-yl)-1H-isoindole-1,3(2H)-dione
• CAS NO: 7065-05-6
• Molecular Formula: C₁₂H₁₁NO₂
• Molecular Weight: 201.22124
• Mol File: 7065-05-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 595.9°Cat760mmHg
• Flash Point: 314.2°C
• Appearance: /
• Density: 1.32g/cm³
• Vapor Pressure: 3.64E-14mmHg at 25°C
• Refractive Index: 1.65
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(but-3-en-2-yl)isoindoline-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(but-3-en-2-yl)isoindoline-1,3-dione(7065-05-6)
• EPA Substance Registry System: 2-(but-3-en-2-yl)isoindoline-1,3-dione(7065-05-6)

Safety Data

• Hazardous Substances Data: 7065-05-6(Hazardous Substances Data)

Usage

General Description

The chemical 2-(but-3-en-2-yl)isoindoline-1,3-dione, also known as "2-(E)-But-3-enyl-1,3-dioxoisoindoline", is a compound with the molecular formula C12H11NO2. It is a derivative of isoindoline-1,3-dione, and its structure includes a butenyl group attached to the isoindoline ring. 2-(but-3-en-2-yl)isoindoline-1,3-dione has potential applications in pharmaceuticals and organic synthesis due to its unique structure and reactivity. It is important to handle this chemical with proper precaution and safety measures, as its handling and use may require special expertise and care.

InChI:InChI=1/C31H36N4O4S2/c1-5-7-15-34-27(33-16-13-23(14-17-33)30(38)39-6-2)24(20(3)25(19-32)28(34)36)18-26-29(37)35(31(40)41-26)21(4)22-11-9-8-10-12-22/h8-12,18,21,23H,5-7,13-17H2,1-4H3

Upstream product

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• 88-99-3 benzene-1,2-dicarboxylic acid 
• 136918-14-4 phthalimide 
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• 628-08-0 crotyl acetate 

Downstream Products

• 133787-12-9 α-N-benzoyl-δ-methyl-δ-N-phthaloylornithine methyl ester 
• 213998-00-6 2-(1-methyl-3-phenyl-allyl)-isoindole-1,3-dione 
• 2028-33-3 2-(1-methyl-2-oxo-propyl)-isoindole-1,3-dione 
• 4667-80-5 2-(1,3-dioxoisoindolin-2-yl)butan-4-al 

Relevant articles and documents

Design, synthesis, and evaluation of nonaqueous silylamines for efficient CO2 capture

A series of silylated amines have been synthesized for use as reversible ionic liquids in the application of post-combustion carbon capture. We describe a molecular design process aimed at influencing industrially relevant carbon capture properties, such as viscosity, temperature of reversal, and enthalpy of regeneration, while maximizing the overall CO2-capture capacity. A strong structure-property relationship among the silylamines is demonstrated in which minor structural modifications lead to significant changes in the bulk properties of the reversible ionic liquid formed from reaction with CO 2.

CYCLIZED SULFAMOYLARYLAMIDE DERIVATIVES AND THE USE THEREOF AS MEDICAMENTS FOR THE TREATMENT OF HEPATITIS B

Inhibitors of HBV replication of Formula (I-A), including stereochemically isomeric forms, and salts, hydrates, solvates thereof, wherein Ra to Rd, and R1 to R8 have the meaning as defined herein. The present invention also relates to processes for preparing said compounds, pharmaceutical compositions containing them and their use, alone or in combination with other HBV inhibitors, in HBV therapy.

The synthesis and the chemical and physical properties of non-aqueous silylamine solvents for carbon dioxide capture

Silylamine reversible ionic liquids were designed to achieve specific physical properties in order to address effective CO2 capture. The reversible ionic liquid systems reported herein represent a class of switchable solvents where a relatively non-polar silylamine (molecular liquid) is reversibly transformed to a reversible ionic liquid (RevIL) by reaction with CO2 (chemisorption). The RevILs can further capture additional CO2 through physical absorption (physisorption). The effects of changes in structure on (1) the CO2 capture capacity (chemisorption and physisorption), (2) the viscosity of the solvent systems at partial and total conversion to the ionic liquid state, (3) the energy required for reversing the CO2 capture process, and (4) the ability to recycle the solvents systems are reported.