191110-74-4 Usage
Explanation
The compound's name describes its structure, indicating it is a spirocyclic compound with a diazaspiro[4.5]decane core, two ketone groups (dione), and a phenylmethoxy group attached at the eighth position.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O) atoms in the compound, which are 16, 19, 2, and 3, respectively.
Explanation
The compound contains a phenylmethoxy group (C6H5-O-CH3) attached at the eighth position and two ketone groups (C=O), making it a dione.
Explanation
The compound is derived from 1,3-diazaspiro[5.5]undecane-2,4-dione, with a phenylmethoxy group added at the eighth position.
Explanation
The compound has potential applications in the pharmaceutical industry due to its unique structure and functional groups, making it an interesting candidate for further research and development.
Explanation
The compound's unique structure and functional groups suggest that it may have untapped potential in the field of medicinal chemistry, warranting further research and development to understand its properties and possible applications.
Structure
Spirocycle with a diazaspiro[4.5]decane core
Functional Groups
Phenylmethoxy, Dione
Derivative
1,3-Diazaspiro[5.5]undecane-2,4-dione
Application
Medicinal Chemistry and Drug Development
Field of Interest
Pharmaceutical Industry
Research Potential
Further exploration and development
Check Digit Verification of cas no
The CAS Registry Mumber 191110-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,1,1 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191110-74:
(8*1)+(7*9)+(6*1)+(5*1)+(4*1)+(3*0)+(2*7)+(1*4)=104
104 % 10 = 4
So 191110-74-4 is a valid CAS Registry Number.
191110-74-4Relevant articles and documents
SUBSTITUTED SPIROCYCLIC KETOENOLS
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Page/Page column 131-132, (2008/06/13)
The invention relates to novel substituted spirocyclic ketoenols of formula (I), wherein W, X, Y, Z, A, B, D, and G have the meaning indicated above, several methods for the production thereof, and the use thereof as pesticides, microbiocides, and herbici
