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Bicyclo[2.2.2]octane-1-carboxaldehyde tosylhydrazone is a complex organic compound with the molecular formula C16H21N2O3S. It is derived from bicyclo[2.2.2]octane-1-carboxaldehyde, a bicyclic aldehyde, and tosylhydrazine, a sulfonamide. bicyclo<2.2.2>octane-1-carboxaldehyde tosylhydrazone is characterized by the presence of a tosylhydrazone group, which is formed by the reaction of the aldehyde with tosylhydrazine, leading to the formation of a hydrazone bond. The tosyl group (-SO2C6H4CH3) provides stability to the molecule and can be used as a protecting group in organic synthesis. Bicyclo[2.2.2]octane-1-carboxaldehyde tosylhydrazone is a white crystalline solid and is used as an intermediate in the synthesis of various organic compounds, particularly in the preparation of complex molecules that require the bicyclo[2.2.2]octane core structure. Its stability and reactivity make it a valuable tool in organic chemistry for the construction of molecular frameworks with specific stereochemistry and functional groups.

7363-97-5

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7363-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7363-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7363-97:
(6*7)+(5*3)+(4*6)+(3*3)+(2*9)+(1*7)=115
115 % 10 = 5
So 7363-97-5 is a valid CAS Registry Number.

7363-97-5Downstream Products

7363-97-5Relevant academic research and scientific papers

Bicyclonon-1-ene: Matrix Isolation and Spectroscopic Characterization of a Moderately Strained Bridgehead Olefin

Gudipati, Murthy S.,Radziszewski, Juliusz G.,Kaszynski, Piotr,Michl, Josef

, p. 3668 - 3674 (2007/10/02)

Bicyclonon-1-ene was generated in low-temperature matrices and in fluid solutions by photodecomposition of bicyclooct-1-yldiazomethane and its photorearrangement product, 3-(bicyclooct-1-yl)diazirine.It was characterized by IR and UV absorption and by 1H and 13C NMR spectroscopy.Further evidence for the proposed structure was provided by self-trapping and by the spectral effects of deuteration on the olefinic carbon.Observed IR spectra and isotopic shifts agree well with the results of semiempirical (MNDO) and ab initio (SCF/6-31G*) calculations.

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