253324-90-2 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-1-(hydroxyimino)-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as a potential therapeutic agent for its anti-inflammatory and anti-tumor properties. Its ability to modulate inflammatory responses and inhibit tumor growth makes it a promising candidate for the development of new drugs to treat various inflammatory and cancer-related conditions.
Used in Enzyme Inhibition:
(Z)-1-(hydroxyimino)-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as an enzyme inhibitor, targeting specific enzymes involved in various biological processes. Its inhibitory effects can be harnessed to develop drugs that modulate enzyme activity, potentially leading to the treatment of enzyme-related disorders.
Used in Receptor Antagonism:
(Z)-1-(hydroxyimino)-3-methyl-4,5-dihydro-1H-benzo[d]azepin-2(3H)-one is used as a receptor antagonist, blocking the action of specific receptors in the body. This property can be utilized to develop drugs that interfere with receptor-mediated signaling pathways, offering new therapeutic approaches for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 253324-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,3,2 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 253324-90:
(8*2)+(7*5)+(6*3)+(5*3)+(4*2)+(3*4)+(2*9)+(1*0)=122
122 % 10 = 2
So 253324-90-2 is a valid CAS Registry Number.
253324-90-2Relevant academic research and scientific papers
METHOD FOR PRODUCING BENZAZEPINONE
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Page/Page column 17-18, (2008/12/04)
It is an object of the present invention to provide 2-iminocarboxylic acid derivatives, and a practically suitable industrial method for producing benzazepinones in a short process under mild conditions. The present invention provides a method for producing a benzazepinone or a salt thereof, which comprises opening a ring of an isoquinoline derivative and subsequently converting the thus generated amine into a benzazepinone through lactamization reaction.
