5228-33-1 Usage
Uses
Used in Pharmaceutical Industry:
Methyl azepane-2-carboxylate is used as a building block for the synthesis of various bioactive molecules, contributing to the development of new drugs for neurological and psychiatric disorders. Its unique chemical structure allows for the creation of compounds with potential therapeutic applications.
Used in Drug Development:
Methyl azepane-2-carboxylate is utilized as a key intermediate in the development of new drugs, particularly for neurological and psychiatric disorders. Its presence in the molecular structure of these drugs aids in enhancing their efficacy and targeting specific biological pathways.
Used in Organic Compound Production:
Methyl azepane-2-carboxylate serves as an intermediate in the production of other organic compounds, such as agrochemicals and flavoring agents. Its versatility in chemical reactions enables the synthesis of a diverse range of compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5228-33-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5228-33:
(6*5)+(5*2)+(4*2)+(3*8)+(2*3)+(1*3)=81
81 % 10 = 1
So 5228-33-1 is a valid CAS Registry Number.
5228-33-1Relevant academic research and scientific papers
PTERIDINONES AS INHIBITORS OF POLO - LIKE KINASE
-
, (2011/07/09)
The present invention provides compounds having a structure according to Formula (I) or a salt or solvate thereof, wherein ring A, X, R1, R2, R3, R4, R5 and R6, are defined herein. The invention further provides pharmaceutical compositions including the compounds of the invention and methods of making and using the compounds and compositions of the invention, e.g., in the treatment and prevention of various disorders, such as Parkinson's disease.
REACTION OF SCHIFF BASES ANIONS WITH α,ω-DIHALOALKENES : SYNTHETIC ROUTE TO CYCLIC α-AMINOACID DERIVATIVES.
Joucla, M.,Goumzili El, M.
, p. 1681 - 1684 (2007/10/02)
Imine anions of α-aminoesters, obtained from LDA/THF, undergo copper-catalyzed substitution reactions with α,ω-dihaloalkanes to lead to ω-haloalkylimines which are converted to cyclic α-aminoacid derivatives under anionic and thermal conditions.
