18409-76-2 Usage
White to off-white powder
This describes the physical appearance of the compound.
Used for psychoactive and sedative effects
The compound is known for its ability to alter perception, mood, and behavior, as well as its calming and relaxing effects.
Derivative of isoindoline
This indicates that the compound is derived from the bicyclic organic compound isoindoline.
Contains an ethanol group
This indicates the presence of an ethanol group in the compound's structure.
Not approved for medical or industrial use
The compound is not currently used for any approved medical or industrial purposes.
Of interest for research purposes
The compound is of interest to researchers due to its psychoactive properties.
Potential candidate for pharmaceutical development
The compound's psychoactive properties make it a potential candidate for the development of new pharmaceuticals, particularly for the treatment of neurological and psychiatric disorders.
Strictly regulated and controlled
Due to its psychoactive effects, the compound is subject to strict regulations and controls to prevent its potential abuse and misuse.
Check Digit Verification of cas no
The CAS Registry Mumber 18409-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,0 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18409-76:
(7*1)+(6*8)+(5*4)+(4*0)+(3*9)+(2*7)+(1*6)=122
122 % 10 = 2
So 18409-76-2 is a valid CAS Registry Number.
18409-76-2Relevant academic research and scientific papers
Synthesis of Some 2,5-Benzoxazocine and 2,6-Benzoxazonine Derivatives from ω-(Dihydroisoindol-2-yl)alkanol Precursors by Means of Cyanogen Bromide
Bremner, John B.,Thirasasana, Narumol
, p. 2307 - 2314 (2007/10/02)
Reaction of cyanogen bromide with 2-(1-phenyl-2,3-dihydro-1H-isoindol-2-yl)ethanol (5a) gave 1-phenyl 3,4,5,6-tetrahydro-1H-2,5-benzoxazocine-5-carbonitrile (6a) in a low to moderate yield..Similarly, 3-(1-phenyl-2,3-dihydro-1H-isoindol-2-yl)propan-1-ol (5c) gave 1-phenyl-1,3,4,5,6,7-hexahydro-2,6-benzoxazonine-6-carbonitrile (6c).The analogous 1-(4-methoxyphenyl) derivatives of both medium ring systems were also prepared, and some mechanistic aspects of the results are discussed.Conversion of (6a) into the analgesic, Nefopam, is described.
