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3-Oxa-9-azatricyclo[3.3.1.02,4]nonane, also known as (1alpha,2beta,4beta,5alpha)-(9CI), is a complex organic compound with a unique cyclic structure. It is composed of three carbon atoms forming a tricyclo ring system, with one oxygen atom (the "oxa" part) and one nitrogen atom (the "aza" part) incorporated into the structure. The compound is characterized by its specific stereochemistry, with the 1alpha, 2beta, 4beta, and 5alpha configurations indicating the spatial arrangement of the atoms. This chemical is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of stereochemistry. It may also have potential applications in the development of pharmaceuticals or other specialty chemicals, although specific uses would depend on further research and development.

169219-68-5

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169219-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 169219-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,1 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 169219-68:
(8*1)+(7*6)+(6*9)+(5*2)+(4*1)+(3*9)+(2*6)+(1*8)=165
165 % 10 = 5
So 169219-68-5 is a valid CAS Registry Number.

169219-68-5Downstream Products

169219-68-5Relevant academic research and scientific papers

Synthesis of exo- and endo-6,7-epoxytropanes

Justice, David E.,Malpass, John R.

, p. 11963 - 11976 (2007/10/03)

Diastereoisomeric N-protected 2,3-epoxy-4-amino-cycloheptanols are synthesised; cyclisation of derivatives provides a practical route to N-protected exo-(β)-6,7-epoxynortropanes and the first endo-(α-)-6,7-epoxynortropane. Hydride reduction gives the corr

Exo- and Endo-6-Hydroxy- and 6,7-Epoxytropanes; Total Synthesis of Scopine, Pseudoscopine, and Nor- Derivatives

Justice, David E.,Malpass, John R.

, p. 4689 - 4692 (2007/10/02)

Novel endo- 6,7-epoxy-8-azabicyclooctane derivatives and the corresponding exo-analogues have been synthesised and show substantially different reactivity; the resistance of the exo-epoxides to ring opening during hydride reduction and catalytic hydrogenolysis is exploited in a total synthesis of scopine, pseudoscopine, and nor- derivatives.

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