697-25-6 Usage
Description
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid, also known as norbornane-1-carboxylic acid, is a bicyclic organic compound with a unique molecular structure characterized by a fused bicyclic system. It is known for its stability and structural rigidity conferred by the norbornane framework, making it a valuable compound in various applications.
Uses
Used in Pharmaceutical Industry:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a starting material for the synthesis of various drugs and bioactive molecules due to its unique molecular structure and properties.
Used in Chemical Research:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a subject for studies in molecular modeling and stereochemistry, taking advantage of its conformational flexibility and stereochemical properties.
Used in Organic Synthesis:
Tricyclo[2.2.1.0~2,6~]heptane-1-carboxylic acid is used as a key intermediate in the synthesis of complex organic compounds, leveraging its stability and structural attributes for the development of novel chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 697-25-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 697-25:
(5*6)+(4*9)+(3*7)+(2*2)+(1*5)=96
96 % 10 = 6
So 697-25-6 is a valid CAS Registry Number.
697-25-6Relevant articles and documents
Monoamine oxidase-catalyzed oxidation of endo,endo-2-amino-6-[(Z)-2'-phenyl]ethenylbicyclo[2.2.1]heptane, a potential probe for a radical cation intermediate
Wang, Xueqing,Silverman, Richard B.
, p. 1645 - 1651 (2007/10/03)
An 11-step synthesis of endo,endo-2-amino-6-[(E)-2'-phenyl]ethenylbicyclo[2.2.1]heptane (6) and the corresponding (Z)-isomer (7) was carried out in an attempt to make a compound that could trap the purported amine radical cation intermediate during monoamine oxidase (MAO)-catalyzed oxidation of amines. The E-isomer was not a substrate for MAO, and the Z-isomer was a very poor substrate. No trapping product was observed. Possible explanations for the inability of these compounds to trap a potential radical cation intermediate are discussed. Copyright (C) 2000 Elsevier Science Ltd.