98334-44-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
A spiro compound is characterized by the fusion of two or more rings in such a way that they share a single common atom.
Explanation
The compound has a 1,3-diazaspiro backbone, which is a specific arrangement of nitrogen atoms within the spiro structure.
Explanation
The compound contains a thione functional group (C=S), which is a sulfur analog of a carbonyl group (C=O).
Explanation
The compound has potential applications in the development of drugs targeting specific biological pathways due to its unique structure and functional groups.
Explanation
The spiro structure and thione moiety make the compound a point of interest for researchers exploring new chemical scaffolds for designing and developing drugs.
Explanation
Additional research and investigations on the compound's properties and reactivity will provide valuable insights into its potential biological and pharmaceutical applications.
Explanation
The 6CI (Chemical Information) code is a unique identifier assigned to the compound in a chemical database, which helps in organizing and retrieving information about the compound.
Spiro compound
Yes
Unique backbone
1,3-diazaspiro
Thione functional group
Present
Potential applications
Medicinal chemistry
Research interest
Novel chemical scaffolds for drug design and development
Further studies
Properties and reactivity
Chemical classification
6CI
Check Digit Verification of cas no
The CAS Registry Mumber 98334-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,3,3 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98334-44:
(7*9)+(6*8)+(5*3)+(4*3)+(3*4)+(2*4)+(1*4)=162
162 % 10 = 2
So 98334-44-2 is a valid CAS Registry Number.
98334-44-2Relevant academic research and scientific papers
Synthesis, spectroscopic characterization and ab initio investigation of thioanalogues of spirohydantoins
Marinov, Marin,Minchev, Stoyan,Stoyanov, Neyko,Ivanova, Galya,Spassova, Milena,Enchev, Venelin
, p. 9 - 16 (2007/10/03)
Dithioanalogues of cycloalkanespiro-5-hydantoins were prepared by reaction of the respective spirohydantoins with Lawesson's reagent or P4S 10. Cycloalkanespiro-5-(2-thiohydantoins) and cycloalkanespiro-5-(4- hydantoins) were also synthesized from cycloalkanespiro-5-(2,4-dithiohydantoins) via different reaction pathways. The structures of the compounds obtained were verified by 1H, 13C NMR and IR spectroscopy. Quantum-chemical calculations at the ab initio level of molecular nonlinear characteristics were performed. Increase of polarizability α and the second hyperpolarizability ? with enlarging the saturated ring was observed in all the structures studied.
