188192-55-4 Usage
Explanation
The compound consists of 7 carbon atoms, 15 hydrogen atoms, and 1 nitrogen atom.
Explanation
This name is derived from its structure, indicating a methyl group attached to a six-membered azepine ring with an amine group at the 3-position.
Explanation
Azepines are a group of heterocyclic compounds with a seven-membered ring containing one nitrogen atom.
Explanation
The compound has a six-membered ring structure with a methyl group (CH3) attached to it, indicating the presence of six hydrogen atoms in the ring.
Explanation
1H-Azepin-3-amine, hexahydro-1-methyl is commonly used in the pharmaceutical industry to synthesize a range of drugs for medical purposes.
Explanation
This chemical may pose health risks if not managed correctly, so it is essential to handle and use it with care to avoid potential hazards.
Class of organic compounds
Azepines
Hexahydro substitution
Methyl group attached to a six-membered ring
Pharmaceutical applications
Synthesis of various drugs
Potential health hazards
Proper handling and usage required
Check Digit Verification of cas no
The CAS Registry Mumber 188192-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,1,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188192-55:
(8*1)+(7*8)+(6*8)+(5*1)+(4*9)+(3*2)+(2*5)+(1*5)=174
174 % 10 = 4
So 188192-55-4 is a valid CAS Registry Number.
188192-55-4Relevant academic research and scientific papers
A novel series of N-(hexahydro-1,4-diazepin-6-yl) and N-(hexahydroazepin-3-yl)benzamides with high affinity for 5-HT3 and dopamine D2 receptors
Hirokawa, Yoshimi,Morie, Toshiya,Yamazaki, Hiroshi,Yoshida, Naoyuki,Kato, Shiro
, p. 619 - 624 (2007/10/03)
A novel series of benzamides with a hexahydro-1,4-diazepine or hexahydroazepine ring in the amine moiety were prepared, and their binding affinities for 5-HT3 and dopamine 4 receptors were evaluated. The R isomer of the 1-ethyl-4-methylhexahydro-1,4-diazepinylbenzamide (R)-22 had potent affinity for both receptors. The R-enantiomer of the corresponding 1-ethylhexahydroazepinylbenzamide 28 showed potent affinity for dopamine D2 receptors with reduced affinity for 5-HT3 receptors, while the S isomer was found to be a potent and selective 5-HT3 receptor antagonist.
