1239589-52-6 Usage
General Description
The chemical "tert-butyl 6-aminospiro[3..." is a synthetic molecule with a spirocyclic structure. It is a derivative of tert-butyl and contains an amino group within the spirocycle. tert-butyl 6-aminospiro[3... may have potential applications in the field of medicinal chemistry or pharmacology, as spirocyclic compounds are often studied for their biological and pharmacological activities. The specific properties and potential uses of this compound would depend on its exact structure and behavior. Further research and analysis would be necessary to determine its potential applications and impact.
Check Digit Verification of cas no
The CAS Registry Mumber 1239589-52-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,5,8 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1239589-52:
(9*1)+(8*2)+(7*3)+(6*9)+(5*5)+(4*8)+(3*9)+(2*5)+(1*2)=196
196 % 10 = 6
So 1239589-52-6 is a valid CAS Registry Number.
1239589-52-6Relevant articles and documents
Cyclobutane-derived diamines: Synthesis and molecular structure
Radchenko, Dmytro S.,Pavlenko, Sergiy O.,Grygorenko, Oleksandr O.,Volochnyuk, Dmitriy M.,Shishkina, Svitlana V.,Shishkin, Oleg V.,Komarov, Igor V.
experimental part, p. 5941 - 5952 (2010/11/04)
Cyclobutane diamines (i.e., cis- and trans-1,3-diaminocyclobutane, 6-amino-3-azaspiro[3.3]heptane, and 3,6-diaminospiro[3.3]heptane) are considered as promising sterically constrained diamine building blocks for drug discovery. An approach to the syntheses of their Boc-monoprotected derivatives has been developed aimed at the preparation of multigram amounts of the compounds. These novel synthetic schemes exploit classical malonate alkylation chemistry for the construction of cyclobutane rings. The conformational preferences of the cyclobutane diamine derivatives have been evaluated by X-ray diffraction and compared with the literature data on sterically constrained diamines, which are among the constituents of commercially available drugs.
