188570-15-2 Usage
Type of Compound
Heterocyclic
Contains a benzene ring fused to a seven-membered ring with nitrogen, making it a complex cyclic structure.
Bicyclic Structure
Yes
The compound has two cyclic structures, which are the benzene ring and the seven-membered ring.
Derivative
Benzazepine
It is derived from the parent compound benzazepine, which is a known chemical structure.
Usage
Research Chemical in Pharmaceutical Industry
Commonly used in research and development for potential therapeutic applications.
Potential Applications
Treatment of neurological and psychiatric disorders
Derivatives of 1H-2-Benzazepine, 2,3,4,5-tetrahydro-2-methyl- have been studied for their potential use in treating various disorders related to the nervous system.
Ongoing Research
Pharmacological and therapeutic potential
Further studies are being conducted to explore the compound's properties and its possible uses in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 188570-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,5,7 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188570-15:
(8*1)+(7*8)+(6*8)+(5*5)+(4*7)+(3*0)+(2*1)+(1*5)=172
172 % 10 = 2
So 188570-15-2 is a valid CAS Registry Number.
188570-15-2Relevant academic research and scientific papers
Narita, Ken,Shirai, Naohiro,Sato, Yoshiro
, p. 2544 - 2549 (1997)
2-Methyl-2-[(trimethylsilyl)methyl]-2,3,4,5,6,7-hexahydro-1H-2- benzazoninium iodide (9), 2-methyl- 2-[(trimethylsilyl)methyl]-1,2,3,4,5,6-hexahydro-2-benzazocinium iodide (15), and 2-methyl-2-[(trimethylsilyl)methyl]-2,3,4,5-tetrahydro-1H-2-benzazepinium iodide (23) exist as mixtures of two stable conformational isomers (types A and B) in an aprotic solvent at room temperature. The corresponding conformational isomers of N-methylides 10A,B, 16A,B, and 24A,B were generated by fluoride ion-induced desilylation, and their rearrangement was investigated. Type A ylides gave [2,3] sigmatropic rearrangement products (isotoluenes) 11, 17, 18, and 27, while type B ylides gave Stevens rearrangement products 8, 20, and 29 via radical-cleavage and -recombination pathways.
