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(1RS,2SR,7RS,9RS,11SR)-6-aza-11-(carbomethoxymethyl)-9-(phenylthio)-1-<(trimethylsilyl)oxy>tricyclo<5.3.1.02,6>undecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94707-75-2

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94707-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94707-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,7,0 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94707-75:
(7*9)+(6*4)+(5*7)+(4*0)+(3*7)+(2*7)+(1*5)=162
162 % 10 = 2
So 94707-75-2 is a valid CAS Registry Number.

94707-75-2Downstream Products

94707-75-2Relevant academic research and scientific papers

Nucleophilic Substitution with Inversion of Configuration at the Nucleophile

Heathcock, Clayton H.,Geldern, Thomas W., von,Lebrilla, Carlito B.,Maier, Wilhelm F.

, p. 968 - 972 (1985)

Treatment of the tricyclic amino alcohol methanesulfonate 1 with lithium chloride in dimethylformamide gives only the tricyclic chloro amine 2, while similar treatment of 1 with sodium thiophenoxide in DMF produces solely the rearranged skeleton 3.Analogous skeletal rearrangement is seen in the reaction of alcohol 4 with phosphorus oxychloride and in the pyrolysis of the (thiocarbonyl)imidazolide 6.It is proposed that all of these reactions proceed through a tetracyclic azetidinium ion, B, and that thioether 3, chloride 5, and compound 7 are products of kinetic control, while chloride 2 is the product of thermodynamic control (Scheme I and II).It is unusual that chloro amine 5, which is forced to undergo SN2 reaction with net inversion of configuration at nitrogen, is substantially more reactive than its isomer 2, in which the substitution occurs with retention of configuration as the nucleophilic center.Several theoretical calculations have been carried out in order to assess the importance of possible stereoelectronic and steric effects.The marked preference of azetidinium ion B to react at C-4 rather than at C-2 can be nicely explained by steric effects; there is no indication of stereoelectronic control in the reactions of B.

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