897669-44-2 Usage
Molecular Weight
399.5 g/mol
Functional Groups
Piperidine ring
Carboxylic acid groups
Ester groups
Phenylmethyl (benzyl) group
Tert-butyl group
Chemical Structure
A piperidine ring with two carboxylic acid groups, one at position 1 and the other at position 4. The 4-carboxylic acid group is esterified with a phenylmethyl group, and the 1-carboxylic acid group is esterified with a 1,1-dimethylethyl (tert-butyl) group.
Application
Used in the synthesis of pharmaceuticals and organic compounds.
Potential
Building block in the development of novel drugs
Precursor for the synthesis of various organic molecules
Importance
Versatile and valuable starting material for the creation of new pharmacological agents and chemical compounds
Of interest in the pharmaceutical industry for the development of new medications and therapeutic treatments
Biological Activity
Potential biological activity due to its structural diversity.
Field of Interest
Medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 897669-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,6,6 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 897669-44:
(8*8)+(7*9)+(6*7)+(5*6)+(4*6)+(3*9)+(2*4)+(1*4)=262
262 % 10 = 2
So 897669-44-2 is a valid CAS Registry Number.
897669-44-2Relevant articles and documents
PYRAZOLONE COMPOUNDS AS METABOTROPIC GLUTAMATE RECEPTOR AGONISTS FOR THE TREATMENT OF NEUROLOGICAL AND PSYCHIATRIC DISORDERS
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Page/Page column 247; 248, (2008/06/13)
Compounds of Formula (I), wherein R1, R2, R3, R4, R5, R6, X, and n are as defined for Formula (I) in the description, processes for the preparation of the compounds and new intermediates employed in the preparation, pharmaceutical compositions containing the compounds, and the use of the compounds in the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction.