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methyl 1-(4-(tert-butyl)phenyl)-2-methyl-3-phenylcycloprop-2-enecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1313370-86-3

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1313370-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313370-86-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,3,7 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1313370-86:
(9*1)+(8*3)+(7*1)+(6*3)+(5*3)+(4*7)+(3*0)+(2*8)+(1*6)=123
123 % 10 = 3
So 1313370-86-3 is a valid CAS Registry Number.

1313370-86-3Downstream Products

1313370-86-3Relevant academic research and scientific papers

Recyclable heterogeneous metal foil-catalyzed cyclopropenation of alkynes and diazoacetates under solvent-free mechanochemical reaction conditions

Chen, Longrui,Leslie, Devonna,Coleman, Michael G.,Mack, James

, p. 4650 - 4661 (2018/05/30)

Silver and copper foil were found to be effective, versatile and selective heterogeneous catalysts for the cyclopropenation of terminal and internal alkynes under mechanochemical reaction conditions. This methodology enables the functionalization of a wide range of terminal or internal alkynes under ambient, aerobic, and solvent-free conditions. Finally, we have demonstrated a unique and versatile one-pot domino Sonogashira-cyclopropenation mechanochemical reaction for the formation of complex cyclopropenes.

Silver triflate-catalyzed cyclopropenation of internal alkynes with donor-/acceptor-substituted diazo compounds

Briones, John F.,Davies, Huw M. L.

, p. 3984 - 3987 (2011/09/16)

Silver triflate was found to be an efficient catalyst for the cyclopropenation of internal alkynes using donor-/acceptor-substituted diazo compounds as carbenoid precursors. Highly substituted cyclopropenes, which cannot be synthesized directly via rhodium(II)-catalyzed carbenoid chemistry, can now be readily accessed.

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