53343-62-7

Basic information

• Product Name: (1RS,2RS,4RS,5SR,7SR,8SR)-methyl 3,6-dioxatetracyclo[6.1.0.0^2,4.0^5,7]nonane-9-carboxylate
• CAS NO: 53343-62-7
• Molecular Weight: 182.176
• Mol File: 53343-62-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1RS,2RS,4RS,5SR,7SR,8SR)-methyl 3,6-dioxatetracyclo[6.1.0.0^2,4.0^5,7]nonane-9-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (1RS,2RS,4RS,5SR,7SR,8SR)-methyl 3,6-dioxatetracyclo[6.1.0.0^2,4.0^5,7]nonane-9-carboxylate(53343-62-7)
• EPA Substance Registry System: (1RS,2RS,4RS,5SR,7SR,8SR)-methyl 3,6-dioxatetracyclo[6.1.0.0^2,4.0^5,7]nonane-9-carboxylate(53343-62-7)

Safety Data

• Hazardous Substances Data: 53343-62-7(Hazardous Substances Data)

Upstream product

• 32399-46-5 7-(methoxycarbonyl)cycloheptatriene 

Downstream Products

• 112297-63-9 DL-(1α,2α,3β,4α,5β,6α,7α)-2,4-Bis(4-methylphenylsulfonyloxy)-3,5-bis(phenylsulfonylamino)bicyclo<4.1.0>heptan-7-carbonsaeure-methylester 
• 112297-51-5 DL-(1α,2α,3β,4α,5β,6α,7α)-3,5-Diazido-2,4-bis(4-methylphenylsulfonyloxy)bicyclo<4.1.0>heptan-7-carbonsaeure-methylester 
• 112297-64-0 DL-(1α,2α,4α,5β,6α,7α,8α)-6-(4-Methylphenylsulfonyloxy)-3-(phenylsulfonyl)-5-(phenylsulfonylamino)-3-azatricyclo<5.1.0.0^2.4>octan-8-carbonsaeure-methylester 
• 112297-65-1 DL-(1α,2α,3α,5α,6β,7α,8α)-2-(4-Methylphenylsulfonyloxy)-4-(phenylsulfonyl)-6-(phenylsulfonylamino)-4-azatricyclo<5.1.0.0^3,5>octan-8-carbonsaeure-methylester 
• 112297-62-8 DL-(1α,2α,3β,4α,5β,6α,7α)-3,5-Bis(phenylsulfonylamino)-2,4-dihydroxytricyclo<4.1.0>heptan-7-carbonsaeure-methylester 
• 112346-65-3 (1α,2α,4α,5α,7α,8α,9α)-3,6-Bis(phenylsulfonyl)-3,6-diazatetracyclo<6.1.0.0^2,4.0^5,7>nonan-9-carbonsaeure-methylester 

Relevant articles and documents

PHOTOOXYGENATION OF 7-SUBSTITUTED CYCLOHEPTATRIENES

Photooxygenation of 7-substituted cycloheptatrienes, including the Me, Et, iPr, Ph, CN, COOMe, COOEt, and CONH2 groups was studied, and several products among the tropilidene-type (1 and 2) and norcaradiene-type (3 and 4) endoperoxides, o-substituted benzaldehydes (5), diepoxides (6 and 7), and ketoalcohols (8) were obtained.Mechanism of the formations of the products was discussed.Thermal isomerization of the endoperoxides (1, 3 and 4) to the corresponding diepoxides (10, 6 and 7), and the reaction of the endoperoxides (1 and 3) with triethylamine were examined.