1333222-34-6 Usage
General Description
Tert-butyl 4-amino-4-(2-ethoxy-2-oxoethyl)piperidine-1-carboxylate is a chemical compound with the molecular formula C15H28N2O4. It is a derivative of piperidine and contains a tert-butyl group, an amino group, an ethoxy group, and a carboxylate group. tert-butyl 4-amino-4-(2-ethoxy-2-oxoethyl)piperidine-1-carboxylate is commonly used as a building block in organic synthesis and pharmaceutical research. It has potential applications in drug discovery and development due to its unique molecular structure and ability to modulate biological activity. Tert-butyl 4-amino-4-(2-ethoxy-2-oxoethyl)piperidine-1-carboxylate may also have pharmacological properties that make it of interest for further study in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1333222-34-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,2 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1333222-34:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*2)+(3*2)+(2*3)+(1*4)=106
106 % 10 = 6
So 1333222-34-6 is a valid CAS Registry Number.
1333222-34-6Relevant articles and documents
Synthesis method of 1,7-diazaspiro[3.5]nonane-7-tert-butyl formate
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Paragraph 0048-0050, (2021/08/07)
The invention provides a process synthesis method of 1,7-diazaspiro[3.5]nonane-7-tert-butyl formate. The synthesis method comprises the following five steps: 1, reacting a compound 1 with a bromine compound 2 and ammonium acetate by a one-pot method to obtain a compound 2; 2, reducing a compound 3 by using lithium borohydride to obtain a compound 4; 3, using triethylamine is used as alkali, and reacting the compound 4 with p-toluene sulfonyl chloride to generate a compound 5; 4, under the catalysis of potassium iodide, taking cesium carbonate as alkali, and carrying out ring closing on the compound 5 to generate a compound 6; and 5, under the action of magnesium chips, removing p-toluene sulfonyl from the compound 6 to obtain a compound 7. The method mainly solves the technical problem that no method suitable for industrial synthesis exists at present, and has the advantages that raw materials are easy to obtain, the total yield is high, and the method is suitable for industrial production.
