55186-89-5 Usage
Description
1-Benzyl-1,4-diazepan-5-one is an organic compound belonging to the diazepane class, characterized by its fused five-membered nitrogen-containing rings. It is a synthetic intermediate with potential applications in the pharmaceutical industry due to its unique chemical structure and properties.
Uses
1-Benzyl-1,4-diazepan-5-one is used as a chemical intermediate for the synthesis of various pharmaceutical compounds, particularly those with potential therapeutic applications.
Used in Pharmaceutical Industry:
1-Benzyl-1,4-diazepan-5-one is used as a diazepane intermediate for the development of novel drugs targeting specific medical conditions.
Used in Inhibitor Applications:
1-Benzyl-1,4-diazepan-5-one is used as an inhibitor of human nitric oxide synthesis, which can be beneficial in the treatment of conditions where nitric oxide overproduction is a concern, such as certain inflammatory diseases or cardiovascular disorders. By inhibiting nitric oxide synthesis, this compound may help regulate the balance of this important signaling molecule in the body, potentially leading to improved patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 55186-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55186-89:
(7*5)+(6*5)+(5*1)+(4*8)+(3*6)+(2*8)+(1*9)=145
145 % 10 = 5
So 55186-89-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O/c15-12-6-8-14(9-7-13-12)10-11-4-2-1-3-5-11/h1-5H,6-10H2,(H,13,15)
55186-89-5Relevant articles and documents
NOVEL TRIAZINE COMPOUNDS
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Page/Page column 124, (2014/02/16)
The present invention relates to novel triazine compounds of formula (1). The present invention also discloses compounds of formula I along with other pharmaceutical ac-ceptable excipients and use of the compounds to modulate the PI3K/ mTOR pathway
PYRAZOLE DERIVATIVE
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Page/Page column 72, (2008/06/13)
Not available
New synthesis of (±)-2-piperazinecarboxylic acid
Merour,Coadou
, p. 2469 - 2470 (2007/10/02)
(±)-2-Piperazinecarboxylic acid is prepared from N-carbethoxy-4-piperidone by α Schmidt rearrangement followed by bromation of the lactam; then α Favorskii rearrangement on the monobromolactam intermediate afforded the desired product.
