81268-07-7

Basic information

• Product Name: anti-3-Methyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid
• Synonyms: anti-3-Methyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid
• CAS NO: 81268-07-7
• Molecular Weight: 281.314
• Mol File: 81268-07-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: anti-3-Methyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid(CAS DataBase Reference)
• NIST Chemistry Reference: anti-3-Methyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid(81268-07-7)
• EPA Substance Registry System: anti-3-Methyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid(81268-07-7)

Safety Data

• Hazardous Substances Data: 81268-07-7(Hazardous Substances Data)

Upstream product

• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 
• 4281-04-3 7-methyl-1,3,5-cycloheptatriene 

Downstream Products

• 81268-10-2 anti-9-Methyl-3,4,11,12-tetraza-exo,endo-tetracyclo<5.3.2.0^2,6.0^8,10>dodec-3-en-11,12-dicarbonsaeure-phenylimid 
• 90857-50-4 5-anti-9-dimethyl-3,4,11,12-tetraza-exo,endo-tetracyclo<5.3.2.0^2,6.0^8,10>dodec-3-ene-11,12-dicarboxylic acid phenylimide 
• 90652-69-0 anti-3,7-dimethyl-9,10-diaza-endo,exo-tetracyclo<3.3.2.0^2,4.0^6,8>decane-9,10-dicarboxylic acid phenylimide 
• 90652-78-1 anti-3,7,7-trimethyl-9,10-diaza-endo,exo-tetracyclo<3.3.2.0^2,4.0^6,8>decane-9,10-dicarboxylic acid phenylimide 
• 81268-17-9 anti-3-Methyl-9,10-diaza-endo,exo-tetracyclo<3.3.2.0^2,4.0^6,8>decan-9,10-dicarbonsaeure-phenylimid 
• 81268-15-7 C₁₇H₁₇N₅O₂ 
• 81268-22-6 anti-3,8-Dimethyl-6,7-diaza-exo-tricyclo<3.2.2.0^2,4>non-8-en-6,7-dicarbonsaeure-phenylimid 
• 90652-59-8 5,5,anti-9-trimethyl-3,4,11,12-tetraza-exo,endo-tetracyclo<5.3.2.0^2,6.0^8,10>dodec-3-ene-11,12-dicarboxylic acid phenylimide 

Relevant articles and documents

Synthesis and Valence Tautomerism of 4(8)-Monosubstituted Homotropilidenes

A synthesis of 4(8)-monosubstituted homotropilidenes (bicycloocta-2,5-dienes) is described, which starts from the Diels-Alder adducts 10b - e of 7-monosubstituted cycloheptatrienes and diazomethane.The same synthetic goal is reached by starting from the Diels-Alder adduct 10a of cycloheptatriene itself and diazoethane, though with the opposite substituent position on the homotropilidene framework.Along this route, endo-8-methyl-, endo-8-isopropyl-, endo-8-phenyl- and exo-8-methylhomotropilidene have been made which display a more or less pronounced valence tautomerism.