6971-11-5

Basic information

• Product Name: 2-(prop-2-en-1-yl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione
• Synonyms: 4-(Prop-2-en-1-yl)-4-azatricyclo-[5.2.1.06]dec-8-ene-3,5-dione;4-(prop-2-en-1-yl)-4-azatricyclo[5.2.1.0^{2,6}]dec-8-ene-3,5-dione
• CAS NO: 6971-11-5
• Molecular Formula: C₁₂H₁₃NO₂
• Molecular Weight: 203.2371
• Mol File: 6971-11-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 377.9°C at 760 mmHg
• Flash Point: 179.7°C
• Density: 1.224g/cm³
• Vapor Pressure: 6.54E-06mmHg at 25°C
• Refractive Index: 1.573
• CAS DataBase Reference: 2-(prop-2-en-1-yl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(prop-2-en-1-yl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione(6971-11-5)
• EPA Substance Registry System: 2-(prop-2-en-1-yl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione(6971-11-5)

Safety Data

• Hazardous Substances Data: 6971-11-5(Hazardous Substances Data)

Usage

Chemical class

Tetrahydroisoindole

Molecular weight

233.3 g/mol

Physical appearance

Pale yellow to beige powder

Solubility

Sparingly soluble in water

Usage

Building block for the synthesis of biologically active molecules in organic synthesis and pharmaceutical research

Potential properties

Medicinal

Therapeutic applications

Under investigation

Upstream product

• 107-11-9 1-amino-2-propene 
• 129-64-6 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride 

Downstream Products

• 2973-17-3 N-allylmaleic imide 

Relevant articles and documents

Preparation method of modified silane coupling agent

A preparation method of a modified silane coupling agent comprises: (1), dissolving mono-anhydride or tetracid dianhydride in glacial acetic acid, adding allylamine according to a molar ratio of the mono-anhydride or tetracid dianhydride to the allylamine being 1:1 or 1:2, stirring and reflowing for 3-24 h, adding water, filtering, washing, and drying to obtain an imide product; (2), dissolving the imide product in an aprotic solvent of medium polarity, adding 0.2 ml or 0.35 ml of a catalyst and trialkoxysilane according to a molar ratio to the imide product being 1:1 or 2:1, and reacting at 50-70 DEG C for 5-48 h, distilling at reduced pressure to remove a low-boiling-point fraction to obtain a product.Least catalyst is used at the premise of ensuring optimal catalytic efficiency so that lowest production cost is achieved.