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p-toluolsulfonsaeure-<6-endo-cyan-2-exo-norbornyl>ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72173-63-8

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72173-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72173-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,7 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72173-63:
(7*7)+(6*2)+(5*1)+(4*7)+(3*3)+(2*6)+(1*3)=118
118 % 10 = 8
So 72173-63-8 is a valid CAS Registry Number.

72173-63-8Relevant academic research and scientific papers

Die Synthese von 6exo-substituierten p-Toluolsulfonsaeure-estern

Fischer, Walter,Grob, Cyril A.,Sprecher, Georg von,Waldner, Adrian

, p. 816 - 823 (1980)

The preparation of hitherto unknown p-toluenesulfonates of 6exo-substituted 2endo-norbornanols is described.

Rearrangements of 5- and 6-Cyano-2-norbornyl Cations

Fermann, Michael,Herpers, Ekkehard,Kirmse, Wolfgang,Neubauer, Regina,Renneke, Franz-Josef,et al.

, p. 975 - 984 (2007/10/02)

Hydroboration of the 5-norbornene-2-carbonitriles 11 afforded 5- and 6-hydroxynorbornane-2-carbonitriles (9a, 10a) along with the analogous ketones 12, 13. 5- and 6-aminonorbornane-2-carbonitriles (17a, 18a) were obtained either from the endo-brosylates 1

Synthese und Hydrolyse von 6endo-substituierten p-Toluolsulfonsaeure-estern.

Grob, Cyril A.,Guenther, Bettina,Hanreich, Reinhard

, p. 2288 - 2298 (2007/10/02)

The Synthesis and Hydrolysis of 6endo-Substituted 2endo-Norbornyl p-Toluenesulfonates; The hydrolysis products of the p-toluenesulfonates of several hitherto unknown 6endo-substituted 2endo-norbornanols have been determined.

Norbornanes. Part 10. Solvolysis of the Stereoisomeric 6-cyano-2-norbornyl p-Toluenesulfonates. A Correction

Grob, Cyril A.,Herzfeld, Danielle

, p. 2443 - 2447 (2007/10/02)

The solvolysis products of the stereoisomeric 6-cyano-2-norbornyl p-toluenesulfonates 1-4 (R = CN) in dioxane/water 7 : 3 have been determined.In contrast to an earlier report the 6exo-cyano-2exo-norbornyl p-toluenesulfonate (1; R = CN) yields 30percent of the 2endo-alcohol 9 (R = CN) beside the 2exo-alcohol 10 and the norbornenes 12 and 13.The results confirm that -I substituents at C(6) reduce 1,3-bridging in the intermediate norbornyl cation and hence its rate of rearrangement.The relatively high rate constants for some 6-fluoro- and 6-cyano-2exo-norbornyl p-toluenesulfonates are ascribed to C,C-hyperconjugation assisted by the conjugative effects of the 6-fluoro and cyano substituents.

The Synthesis of 6-substituted 2-Norbornanols

Grob, Cyril A.,Guenther, Bettina,Waldner, Adrian

, p. 2709 - 2720 (2007/10/02)

The preparation of several 6-exo- and 6-endo-substituted 2-exo- and 2-endo-norbornanols and their p-toluenesulfonates is described.

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