5852-57-3 Usage
Molecular structure
A complex structure containing a spirocyclic ring system with a thiocarbonyl group, derived from a 1,2,4-triazole core.
Spirocyclic ring system
The compound has a unique arrangement of atoms in the form of a closed loop or ring, which includes both carbon and sulfur atoms.
Thiocarbonyl group
A functional group consisting of a double-bonded carbon atom and a sulfur atom, which contributes to the compound's chemical reactivity and properties.
1,2,4-Triazole core
The central core of the molecule, which is composed of three nitrogen atoms and one carbon atom, forming a five-membered ring structure.
2,3-Dimethylphenyl substituent
A functional group consisting of a phenyl ring (a six-membered carbon ring with alternating single and double bonds) with two methyl groups (CH3) attached to the 2nd and 3rd carbon positions, which affects the compound's steric properties and reactivity.
7-Methyl substituent
A methyl group (CH3) attached to the 7th carbon position of the triazaspirodecane ring, further contributing to the compound's complexity and properties.
Potential applications
The compound may have possible uses in pharmaceuticals or materials science due to its unique structure and properties.
Synthesis and reactivity
Researchers in the field of organic chemistry may be interested in the synthesis methods and chemical reactivity of this compound, as it could lead to the development of new compounds or reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 5852-57-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,5 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5852-57:
(6*5)+(5*8)+(4*5)+(3*2)+(2*5)+(1*7)=113
113 % 10 = 3
So 5852-57-3 is a valid CAS Registry Number.
5852-57-3Relevant articles and documents
Synthesis of a Homologous Series of Trialkyl Arsines (C3-C12) and Applications of Arsenic Triiodide as a Synthetic Precursor
Ligiéro, Carolina B.P.,Francisco, Marcos A.S.,Gama, Michelle S.,Carbonezi, Carlos A.,Leocadio, Isabela C.L.,de Souza, Wladmir F.,Esteves, Pierre M.
, p. 912 - 916 (2021/03/17)
This work presents some modifications in the post-synthetic processing for a classical arsenic reagent: AsI3. In comparison with the widely used analog, the trichloride, arsenic triiodide presents several advantages such as low toxicity, air stability, and low volatility. It was used as a synthetic precursor in the preparation of a variety of arsenic(III) derivatives like arsines, arsenites, and thioarsenites. Besides that, AsI3 was submitted to a diversity-oriented Grignard reaction in the preparation of a homologous series of trialkyl arsines ranging from AsC3H9 to AsC12H27. The series was analyzed by comprehensive two-dimensional gas chromatography coupled with time-of-flight mass spectrometry to provide a trialkyl arsines library that can be used for the direct analysis of natural samples.
