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1176868-52-2

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1176868-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1176868-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,6,8,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1176868-52:
(9*1)+(8*1)+(7*7)+(6*6)+(5*8)+(4*6)+(3*8)+(2*5)+(1*2)=202
202 % 10 = 2
So 1176868-52-2 is a valid CAS Registry Number.

1176868-52-2Downstream Products

1176868-52-2Relevant academic research and scientific papers

Developing a diastereoselective intramolecular [4 + 3] cycloaddition of nitrogen-stabilized oxyallyl cations derived from N-sulfonyl-substituted allenamides

Lohse, Andrew G.,Hsung, Richard P.,Leider, Mitchell D.,Ghosh, Sunil K.

experimental part, p. 3246 - 3257 (2011/07/09)

Efforts toward achieving a practical and diastereoselective intramolecular [4 + 3] cycloaddition of nitrogen-stabilized oxyallyl cations with tethered dienes are described. Epoxidation of N-sulfonyl substituted allenamides with dimethyldioxirane (DMDO) generates nitrogen-stabilized oxyallyl cations that readily undergo stereoselective [4 + 3] cycloaddition with dienes. Selectivity is found to depend on the tethering length as well as the stability of the oxyallyl cation intermediate, whether generated from N-carbamoyl- or N-sulfonyl-substituted allenamides. The use of chiral N-sulfonyl-substituted allenamides provided minimal diastereoselectivity in the cycloaddition, while high diastereoselectivity can be achieved with a stereocenter present on the tether. These studies provide further support for the synthetic utility of allenamides.

Thermal intramolecular [4 + 2] cycloadditions of allenamides: A stereoselective tandem propargyl amide isomerization-cycloaddition

Lohse, Andrew G.,Hsung, Richard P.

supporting information; experimental part, p. 3430 - 3433 (2009/12/24)

A stereoselective intramolecular normal demand [4 + 2] cycloaddition of allenamides under thermal conditions without metal assistance is described. This work led to the development of a stereoselective tandem propargyl amide-isomerization-[4 + 2] cycloadd

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