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Carbamic acid, [4-(acetyloxy)-2-cyclohepten-1-yl]-, phenylmethyl ester, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113340-08-2

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113340-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113340-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113340-08:
(8*1)+(7*1)+(6*3)+(5*3)+(4*4)+(3*0)+(2*0)+(1*8)=72
72 % 10 = 2
So 113340-08-2 is a valid CAS Registry Number.

113340-08-2Downstream Products

113340-08-2Relevant academic research and scientific papers

Synthetic Approaches to Nortropanes and Nortrop-6-enes; Intramolecular Displacement by Nitrogen in 7-Membered Rings

Naylor, Antoinette,Howarth, Nicola,Malpass, John R.

, p. 451 - 468 (2007/10/02)

The synthesis of simple nortropane and nortrop-6-ene derivatives from cyclohepta-1,3-diene is described.The key intermediates are trans-1-amino-4-chloro-cycloheptanes and -cyclohept-2-enes which are derived efficiently from the corresponding cis-amino-alcohols and undergo intramolecular cyclisation.Corresponding derivatisation of cyclohexa- and cycloocta-1,3-dienes is explored and attempts to achieve Pd-catalysed cyclisation of 1-amino-4-acetoxy-derivatives is described.Nitrogen inversion data for selected nortropane derivatives are included. Key Words: nortropanes/enes; 1,4-disubstitute cyclohexanes, cycloheptanes, cyclooctanes and -enes; intramolecular cyclisation; slow nitrogen inversion.

A SIMPLE APPROACH TO NORTROPANE AND NORTROP-6-ENE DERIVATES

Bathgate, Antoinette,Malpass, John R.

, p. 5937 - 5940 (2007/10/02)

Intramolecular cyclisation of trans-1-(benzylamino)-4-chlorocycloheptane and hept-2-ene gives the corresponding 8-azabicyclo(3.2.1)octane (nortropane) and -oct-6-ene (nortrop-6-ene) derivatives respectively.Under appropriate conditions, cyclohept-1,3-diene is converted into nortropane in 75percent overall yield.

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