24147-30-6

Basic information

• Product Name: 4,7-Methano-1H-isoindole-1,3(2H)-dione, 2-(benzoyloxy)-3a,4,7,7a-tetrahydro-
• CAS NO: 24147-30-6
• Molecular Formula: C16H13NO4
• Molecular Weight: 283.284
• Mol File: 24147-30-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,7-Methano-1H-isoindole-1,3(2H)-dione, 2-(benzoyloxy)-3a,4,7,7a-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 4,7-Methano-1H-isoindole-1,3(2H)-dione, 2-(benzoyloxy)-3a,4,7,7a-tetrahydro-(24147-30-6)
• EPA Substance Registry System: 4,7-Methano-1H-isoindole-1,3(2H)-dione, 2-(benzoyloxy)-3a,4,7,7a-tetrahydro-(24147-30-6)

Safety Data

• Hazardous Substances Data: 24147-30-6(Hazardous Substances Data)

Upstream product

• 21715-90-2 endo-N-hydroxy-5-norbornene-2,3-dicarboxyimide 
• 65-85-0 benzoic acid 
• 99502-89-3 Chlorameisensaeure-N-hydroxy-norborn-5-en-2,3-dicarboximidester 
• 122129-84-4 C₁₇H₁₃NO₆ 
• 129-64-6 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride 
• 5433-80-7 cis-N-sulphonyloxy-5-norbornene-endo-2,3-dicarboximide 
• 98-88-4 benzoyl chloride 

Relevant articles and documents

The use of aminoglycoside derivatives to study the mechanism of aminoglycoside 6′-N-acetyltransferase and the role of 6′-NH2 in antibacterial activity

Aminoglycoside antibiotics act by binding to 16S rRNA. Resistance to these antibiotics occurs via drug modifications by enzymes such as aminoglycoside 6′-N-acetyltransferases (AAC(6′)s). We report here the regioselective and efficient synthesis of N-6′-ac

Base catalysed lossen rearrangement of N-sulphonyloxy-2,3-norborn-5-enedicarboximide

N-Sulphonyloxy-2,3-norborn-5-enedicarboximide 1 underwent Lossen rearrangement with some nucleophilic reagents, but it failed to undergo Beckmann rearrangement.

Zur Stabilitaet von Mischanhydriden des Chlorameisensaeure-N-hydroxy-norborn-5-en-2,3-dicarboximidesters

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