886449-72-5 Usage
General Description
1,7-Diazaspiro[4.5]decane-1-carboxylic acid, 6-oxo-, 1,1-diMethylethyl ester is a chemical compound that is also known as spiro[4.5]decan-6-one. It is often used in the synthesis of various pharmaceutical and agrochemical products. 1,7-Diazaspiro[4.5]decane-1-carboxylic acid, 6-oxo-, 1,1-diMethylethyl ester has been shown to possess antimicrobial, antiviral, and anti-inflammatory properties, making it a potential candidate for drug development. Additionally, it has also been used in the synthesis of various heterocycles and ligands. Its 1,1-diMethylethyl ester form provides improved stability and solubility, making it a useful reagent in organic synthesis.
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 articles and documents
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.
