82203-92-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(1-methoxy-4-phenyl-1,5-dihydro-2H-2,3-benzodiazepin-2-yl)ethanone is used as an active pharmaceutical ingredient for its psychoactive and sedative properties. 1-(1-methoxy-4-phenyl-1,5-dihydro-2H-2,3-benzodiazepin-2-yl)ethanone's benzodiazepine nature suggests potential applications in the treatment of anxiety, insomnia, and other related conditions.
Used in Research and Development:
In the field of research and development, 1-(1-methoxy-4-phenyl-1,5-dihydro-2H-2,3-benzodiazepin-2-yl)ethanone serves as a valuable compound for studying the effects of its structural components on biological systems. Its unique molecular structure allows scientists to explore its interactions with various receptors and enzymes, potentially leading to the discovery of new therapeutic targets and drug candidates.
Used in Chemical Synthesis:
1-(1-methoxy-4-phenyl-1,5-dihydro-2H-2,3-benzodiazepin-2-yl)ethanone can be utilized as a key intermediate in the synthesis of other complex organic molecules. Its versatile structure makes it a suitable candidate for the development of novel compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 82203-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,0 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82203-92:
(7*8)+(6*2)+(5*2)+(4*0)+(3*3)+(2*9)+(1*2)=107
107 % 10 = 7
So 82203-92-7 is a valid CAS Registry Number.
82203-92-7Relevant academic research and scientific papers
The Acylation of 5H-2,3-Benzodiazepines and 4H-Thieno- and 8H-thieno-diazepines. Reactions with Acid Anhydrides and Nucleophiles to give Fused 7-Substituted 1-Acyl-1,2-diazepines
Munro, David P.,Sharp, John T.
, p. 1133 - 1136 (2007/10/02)
The acylation of 4-phenyl-5H-2,3-benzodiazepine (1) and its thieno analogues (2) and (3) with acetic anhydride takes a different course from other 2,3-benzodiazepines having a hydrogen atom or a methyl group at position 4.The latter react at N-3 to give the 3-acyl derivatives (11) but 4-phenyl-2,3-benzodiazepine is acylated at N-2 to give the iminium acetate (12) which reacts with alcohols and thiols to give the derivatives (15) in high yield.The reaction of (12) with hydrogen chloride induces rearrangement to an isoquinoline N-imide (18).
