1621863-51-1 Usage
Description
(2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid, also known as (2S,3S)-2-azabicyclo[2.2.1]hept-5-ene-2-carboxylic acid, is a chemical compound characterized by its bicyclic structure. It features an amino group and a carboxylic acid group, classifying it as an amino acid derivative. Although it is not a naturally occurring amino acid, its unique structural attributes and functional groups have positioned it as a valuable component in the design and synthesis of pharmaceuticals and biologically active molecules. Its utility in organic chemistry and potential in drug development underscore its importance as a versatile chemical compound.
Uses
Used in Pharmaceutical Development:
(2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid is used as a building block for the synthesis of pharmaceuticals due to its unique bicyclic structure and functional groups, which can be leveraged to create new drugs with specific therapeutic properties.
Used in Organic Chemistry:
In the field of organic chemistry, (2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid is used as a versatile intermediate for the synthesis of various organic compounds, taking advantage of its reactive amino and carboxylic acid groups to form diverse molecular structures.
Used in the Development of Biologically Active Molecules:
(2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid is utilized as a key component in the creation of biologically active molecules, capitalizing on its structural features to enhance molecular interactions and biological activity.
Used in Drug Design:
(2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid is employed as a structural element in drug design, where its unique stereochemistry and functional groups contribute to the development of molecules with optimized pharmacological profiles.
Used in Material Science:
In material science, (2S,3S)-3-aminobicyclo[2.2.2]octane-2-carboxylic acid may be used as a component in the development of new materials, potentially influencing properties such as reactivity, stability, or selectivity in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1621863-51-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,8,6 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1621863-51:
(9*1)+(8*6)+(7*2)+(6*1)+(5*8)+(4*6)+(3*3)+(2*5)+(1*1)=161
161 % 10 = 1
So 1621863-51-1 is a valid CAS Registry Number.
1621863-51-1Relevant articles and documents
Syntheses of four enantiomers of 2,3-diendo- and 3-endo-aminobicyclo[2.2.2] oct-5-ene-2-exo-carboxylic acid and their saturated analogues
Palko, Marta,Hanninen, Mikko M.,Sillanpaa, Reijo,Fulop, Ferenc
, p. 15080 - 15093 (2014/01/17)
Ethyl 2,3-diendo-3-aminobicyclo[2.2.2]oct-5-ene-2-carboxylate ((±)-1) was resolved with O,O′-dibenzoyltartaric acid via diastereomeric salt formation. The efficient synthesis of the enantiomers of 2,3-diendo-3-aminobicyclo[2.2.2]oct-5-ene-2-carboxylic aci
