745836-30-0 Usage
Description
ANTI-7-CYANO-2-BENZYL-2-AZABICYCLO[2.2.1]HEPTANE is a bicyclic chemical compound with the molecular formula C15H15N. It features a cyano group and a benzyl group, classifying it within the azabicyclic compounds. Known for its potential biological activities and unique structure, this compound plays a significant role in organic synthesis and pharmaceutical research. Its versatility and importance are recognized across various fields, although it requires careful handling due to potential health hazards.
Uses
Used in Organic Synthesis:
ANTI-7-CYANO-2-BENZYL-2-AZABICYCLO[2.2.1]HEPTANE is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for multiple synthetic pathways, making it a valuable component in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, ANTI-7-CYANO-2-BENZYL-2-AZABICYCLO[2.2.1]HEPTANE is utilized as a starting material or a building block in the design and synthesis of new drugs. Its potential biological activities and structural properties contribute to the discovery of novel therapeutic agents.
Used in Biological Systems Study:
ANTI-7-CYANO-2-BENZYL-2-AZABICYCLO[2.2.1]HEPTANE is also employed in the study of biological systems to understand its interactions with biomolecules and its effects on cellular processes. This research can provide insights into the development of targeted therapies and the exploration of its pharmacological potential.
Check Digit Verification of cas no
The CAS Registry Mumber 745836-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,8,3 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 745836-30:
(8*7)+(7*4)+(6*5)+(5*8)+(4*3)+(3*6)+(2*3)+(1*0)=190
190 % 10 = 0
So 745836-30-0 is a valid CAS Registry Number.
745836-30-0Relevant articles and documents
7-Substituted 2-Azabicyclo[2.2.1]heptanes as key intermediates for the synthesis of novel epibatidine analogues; synthesis of syn- and anti-Isoepiboxidine
Malpass, John R.,White, Richard
, p. 5328 - 5334 (2007/10/03)
Neighboring group participation by the 2-nitrogen in anti-7-bromo-2-benzyl- 2-azabicyclo[2.2.1]heptane allows ready nucleophilic substitution at the 7-position by C, N, O, and halogen nucleophiles and opens the way to a range of novel 7-substituted 2-azab
