666256-76-4 Usage
Description
2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI) is a bicyclic chemical compound with the molecular formula C9H9NO. It features a four-membered nitrogen-containing ring fused to a six-membered carbon ring, along with a propynyl group attached to the nitrogen atom. As a chiral compound with the (1S,4R) configuration, it holds potential for pharmaceutical synthesis and as a building block for other organic compounds. Its possible biological activity also makes it a subject of interest for research in pharmacology and medicinal chemistry.
Uses
Used in Pharmaceutical Synthesis:
2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI) serves as a valuable intermediate in the synthesis of pharmaceuticals due to its unique bicyclic structure and chiral configuration. It can be utilized to create a variety of medicinal compounds with potential therapeutic applications.
Used as a Building Block in Organic Synthesis:
In the field of organic chemistry, 2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI) acts as a key building block for the assembly of more complex organic molecules. Its distinct structure allows for the development of novel compounds with specific properties and functions.
Used in Medicinal Chemistry Research:
2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI)'s potential biological activity and unique structural features make it an attractive candidate for further research in medicinal chemistry. It can be explored for its interactions with biological targets, leading to the discovery of new drugs or therapeutic agents.
Used in the Development of Chiral Molecules:
Given its chiral (1S,4R) configuration, 2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI) can be employed in the development of chiral molecules, which are essential in various chemical and pharmaceutical processes. 2-Azabicyclo[2.2.1]hept-5-en-3-one,2-(2-propynyl)-,(1S,4R)-(9CI)'s enantioselective synthesis and properties can be harnessed to create molecules with specific biological activities and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 666256-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,2,5 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 666256-76:
(8*6)+(7*6)+(6*6)+(5*2)+(4*5)+(3*6)+(2*7)+(1*6)=194
194 % 10 = 4
So 666256-76-4 is a valid CAS Registry Number.
666256-76-4Relevant articles and documents
Control of product distribution in the domino metathesis reactions of N-alkynyl 2-azabicyclo[2.2.1]hept-5-en-3-ones. A convenient synthesis of functionalized γ-lactams and indolizidinones
Arjona, Odón,Csák?, Aurelio G.,León, Vanessa,Medel, Rocío,Plumet, Joaquín
, p. 565 - 567 (2007/10/03)
In this report we describe the domino metathesis of N-alkynyl-2-aza-3-oxo- [2.2.1]hept-5-enes. The distribution of products of the domino processes of ROM-CM or ROM-RCM-CM depends on the starting material and on the catalyst used. A sequence of metathesis events has been proposed to account for these results. The procedure can be of use for the synthesis of lactams and indolizidinones.
