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Exo-tricyclo[3.2.1.0-2,4]octane is a cyclic hydrocarbon compound with a unique molecular structure, consisting of three carbon rings fused together in a specific arrangement. The compound is characterized by its exo configuration, which refers to the position of the hydrogen atoms on the outer side of the molecule. This particular arrangement results in a strained and highly reactive molecule, making it an interesting subject for chemical research and potential applications in various fields, such as pharmaceuticals and materials science. The compound's structure and properties make it a valuable tool for studying the effects of ring strain and the behavior of molecules under such conditions.

278-72-8

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278-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 278-72-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 278-72:
(5*2)+(4*7)+(3*8)+(2*7)+(1*2)=78
78 % 10 = 8
So 278-72-8 is a valid CAS Registry Number.

278-72-8Downstream Products

278-72-8Relevant academic research and scientific papers

Competitive Cyclopropanation and Cross-metathesis Reactions of Alkenes Catalysed by Diruthenium Tatrakis Carboxylates

Noels, Alfred F.,Demonceau, Albert,Carlier, Eric,Hubert, Andre J.,Marquez-Silva, Rosa-Linda,Sanchez-Delgado, Roberto A.

, p. 783 - 784 (1988)

Addition of ethyl diazoacetate to a mixture of styrene and norbornene containing a catalytic amount of Ru2(OAc)4 promoted both the cyclopropanation and a selective cross-metathesis of the alkenes.

Nickel-Catalyzed Cyclopropanation with NMe4OTf and nBuLi

Künzi, Stefan A.,Sarria Toro, Juan Manuel,Den Hartog, Tim,Chen, Peter

supporting information, p. 10670 - 10674 (2015/09/02)

Nickel was identified as a catalyst for the cyclopropanation of unactivated olefins by using in situ generated lithiomethyl trimethylammonium triflate as a methylene donor. A mechanistic hypothesis is proposed in which the generation of a reactive nickel carbene explains several interesting observations. Additionally, our findings shed light on a report by Franzen and Wittig published in 1960 that had been retracted later owing to irreproducibility, and provide a rational basis for the systematic development of the reaction for preparative purposes as an alternative to diazomethane or Simmons-Smith conditions.

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