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Cis-1,2,3-triphenyl-cyclopropane is an organic compound with the molecular formula C21H17. It is a cyclic compound consisting of three phenyl rings attached to a cyclopropane ring, with the phenyl rings positioned in a cis configuration, meaning they are on the same side of the cyclopropane ring. cis-1,2,3-Triphenyl-cyclopropan is known for its strained ring structure due to the small size of the cyclopropane ring, which leads to interesting chemical properties and reactivity. It is used in various chemical reactions and as a precursor in the synthesis of other organic compounds. The compound is also notable for its potential applications in materials science and medicinal chemistry, given its unique structure and the ability to influence the properties of molecules it is part of.

795-11-9

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795-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 795-11-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 795-11:
(5*7)+(4*9)+(3*5)+(2*1)+(1*1)=89
89 % 10 = 9
So 795-11-9 is a valid CAS Registry Number.

795-11-9Relevant academic research and scientific papers

Cyclopropane-alkene metathesis by gold(i)-catalyzed decarbenation of persistent cyclopropanes

Mato, Mauro,Martín-Torres, Inmaculada,Herlé, Bart,Echavarren, Antonio M.

, p. 4216 - 4219 (2019/05/06)

A gold(i)-catalyzed cyclopropane-alkene metathesis has been demonstrated with two new families of cyclopropane derivatives of naphthalene and phenanthrene (benzo-fused norcaradienes). In this process, metal carbene units are transferred from a persistent

Gold(I) Carbenoids: On-Demand Access to Gold(I) Carbenes in Solution

Sarria Toro, Juan M.,García-Morales, Cristina,Raducan, Mihai,Smirnova, Ekaterina S.,Echavarren, Antonio M.

supporting information, p. 1859 - 1863 (2017/02/05)

Chloromethylgold(I) complexes of phosphine, phosphite, and N-heterocyclic carbene ligands are easily synthesized by reaction of trimethylsilyldiazomethane with the corresponding gold chloride precursors. Activation of these gold(I) carbenoids with a variety of chloride scavengers promotes reactivity typical of metallocarbenes in solution, namely homocoupling to ethylene, olefin cyclopropanation, and Buchner ring expansion of benzene.

Cyclopropanation with gold(I) carbenes by retro-Buchner reaction from cycloheptatrienes

Solorio-Alvarado, César R.,Wang, Yahui,Echavarren, Antonio M.

, p. 11952 - 11955 (2011/10/04)

Cationic gold(I) promotes the retro-Buchner reaction of 7-substituted 1,3,5-cycloheptatrienes, leading to gold(I) carbenes that cyclopropanate alkenes.

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