35579-33-0 Usage
Chemical class
Spirocycle
Molecular structure
Contains a six-membered ring fused to a dioxane moiety
Functional group
Propiononitrile attached to the six-membered ring
Potential applications
Organic synthesis and pharmaceutical research
Reactivity
Unique reactivity due to its complex structure
Safety concerns
May have hazardous properties and should be handled with caution
Research status
Further research and experimentation are needed to understand potential uses and risks
Molecular weight
Approximately 181.23 g/mol (calculated from the chemical formula)
Appearance
Not provided in the material, but typically appears as a solid or liquid depending on the conditions
Solubility
Not provided in the material, but likely soluble in organic solvents due to its nonpolar nature
Stability
Not provided in the material, but may be sensitive to heat, light, or moisture based on its structure
Regulatory status
Not provided in the material, but it may be subject to specific regulations depending on its intended use and classification as a hazardous substance.
Check Digit Verification of cas no
The CAS Registry Mumber 35579-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,7 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35579-33:
(7*3)+(6*5)+(5*5)+(4*7)+(3*9)+(2*3)+(1*3)=140
140 % 10 = 0
So 35579-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c11-6-2-4-9-3-1-5-10(9)12-7-8-13-10/h9H,1-5,7-8H2
35579-33-0Relevant academic research and scientific papers
STEREOSELECTIVE SYNTHESIS OF THE TRICYCLIC CONDENSED DERIVATIVES OF THIAZOLIDINE
Sokolov, V. V.,Potekhin, A. A.,Ovchinnikova, I. V.,Gindin, V. A.,Smirnov, S. N.
, p. 582 - 589 (2007/10/02)
The perhydro derivatives of thiazoloquinoline, thiazolocyclopentapyridine, thiazoloindole, and cyclopentapyrrolothiazole and also their 2-methyl derivatives were synthesized by the addition of thiirane and methylthiirane at the C=N bond in bicyclic imines of the 2,3,4,4a,5,6,7,8-octahydroquinoline type.An alternative method involves reaction of the thiiranes with amino ketones of the 2,2-ethylenedioxycyclohexylpropylamine type, protected at the carbomyl group, followed by acid deblocking and cyclization by treatment with alkali.The last method is the only method for the production of perhydrocyclopentapyrrolothiazoles, since 2,3,3a,4,5,6-hexahydrocyclopentapyrrole is not a stable imine.Some of the compounds were obtained in the form of single diastereomers, the configurations of which for the two subjects were determined by NMR.In other cases mixtures of the stereoisomers are formed with a srtong preponderance of one of them; arguments concerning their configurations are presented.It is shown that both methods of synthesis lead to an identical stereochemical result.
