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1,4-Methano-1H-isoindole, 3a,4,5,6,7,7a-hexahydro-3a,7a-dimethyl-1,3-diphenyl- is a complex organic compound with a unique molecular structure. It is characterized by a hexahydro-1H-isoindole core, which is a type of bicyclic aromatic compound. The molecule features a 1,4-methano bridge, which connects the two phenyl rings, and a 3a,7a-dimethyl substitution, indicating two methyl groups attached to the 3a and 7a positions of the isoindole ring. 1,4-Methano-1H-isoindole, 3a,4,5,6,7,7a-hexahydro-3a,7a-dimethyl-1,3-diphenyl- is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its specific structural features.

92898-28-7

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92898-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92898-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,9 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92898-28:
(7*9)+(6*2)+(5*8)+(4*9)+(3*8)+(2*2)+(1*8)=187
187 % 10 = 7
So 92898-28-7 is a valid CAS Registry Number.

92898-28-7Downstream Products

92898-28-7Relevant academic research and scientific papers

Intramolecular Diels-Alder Reactions of 3H-Pyrroles Resulting from the Thermal Rearrangements of 2H-Pyrroles

Eddaif, Abdelhamid,Laurent, Andre,Mison, Pierre,Pellissier, Nicole,Carrupt, Pierre-Alain,Vogel, Pierre

, p. 5548 - 5560 (2007/10/02)

The syntheses of methyl- and phenyl-substituted 2H-pyrroles 8 bearing a but-3-enyl or pent-4-enyl side chain are reported.The thermolyses of 8 yielded tricyclic derivatives with the 2-azabicyclohept-2-ene moiety resulting from the intramolecular Di

REACTION DE DIELS-ALDER INTRAMOLECULAIRE DE 3H-PYRROLES

Eddaif, Abdelhamid,Laurent, Andre,Mison, Pierre,Pellissier, Nicole

, p. 2779 - 2782 (2007/10/02)

The first intramolecular Diels-Alder reaction of 3-alkenyl 3H-pyrroles (2-azadiene system) is related.These 3H-pyrroles are in situ generated from 2H-pyrroles.

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