886449-72-5 Usage
Uses
Used in Pharmaceutical Industry:
1,7-Diazaspiro[4.5]decane-1-carboxylic acid, 6-oxo-, 1,1-diMethylethyl ester is used as an intermediate in the synthesis of various pharmaceutical products due to its antimicrobial, antiviral, and anti-inflammatory properties. Its potential as a drug candidate makes it valuable for the development of new treatments.
Used in Agrochemical Industry:
In the agrochemical industry, 1,7-Diazaspiro[4.5]decane-1-carboxylic acid, 6-oxo-, 1,1-diMethylethyl ester is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides, leveraging its antimicrobial and antiviral properties to protect crops.
Used in Organic Synthesis:
1,7-Diazaspiro[4.5]decane-1-carboxylic acid, 6-oxo-, 1,1-diMethylethyl ester is used as a reagent in organic synthesis, particularly in the synthesis of heterocycles and ligands. Its improved stability and solubility in the 1,1-diMethylethyl ester form make it a useful compound for creating complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 886449-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,4,4 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 886449-72:
(8*8)+(7*8)+(6*6)+(5*4)+(4*4)+(3*9)+(2*7)+(1*2)=235
235 % 10 = 5
So 886449-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H26N2O3/c1-5-10-17-11-6-8-16(13(17)19)9-7-12-18(16)14(20)21-15(2,3)4/h5H,1,6-12H2,2-4H3
886449-72-5Relevant academic research and scientific papers
Spirobicyclic diamines 1: synthesis of proline-derived spirolactams via thermal intramolecular ester aminolysis
Kelleher, Fintan,Kelly, Sinead
, p. 3005 - 3008 (2007/10/03)
Proline-derived [4.4]-spirolactams have been synthesised in good yields by a reductive-amination reaction followed by thermal cyclisation of the resulting amine onto the proline ester group in refluxing toluene. The synthesis of the corresponding [4.5]-spirolactams by the same method gave much reduced yields.
