53427-66-0 Usage
Chemical class
1,4-diazepines
Explanation
The compound belongs to the class of 1,4-diazepines, which are a type of diazepine with nitrogen atoms at positions 1 and 4 of the ring.
Explanation
It is an organic compound as it contains carbon and hydrogen atoms.
Explanation
The compound has a six-membered ring containing a nitrogen atom and a seven-membered ring with a nitrogen atom.
Explanation
The hydroxypropyl group indicates the presence of a hydroxyl functional group (-OH) attached to a three-carbon chain (propyl group).
Explanation
Due to the structural characteristics of 1,4-diazepines, which are found in certain classes of psychoactive drugs, the compound may have potential pharmaceutical properties.
Explanation
The compound may have therapeutic effects on the central nervous system, as 1,4-diazepines are known to interact with the central nervous system.
Explanation
More research and studies are required to understand the potential applications and properties of 1-(3-Hydroxypropyl)-2,3,4,5,6,7-hexahydro-1H-1,4-diazepine.
Organic compound
Yes
Ring structure
Six-membered and seven-membered rings
Hydroxypropyl group
Present
Potential pharmaceutical properties
Yes
Therapeutic effects
Central nervous system
Further research needed
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 53427-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53427-66:
(7*5)+(6*3)+(5*4)+(4*2)+(3*7)+(2*6)+(1*6)=120
120 % 10 = 0
So 53427-66-0 is a valid CAS Registry Number.
53427-66-0Relevant academic research and scientific papers
Production of 1-(3-hydroxy-propyl)-1,4-diazepane and 1,4-bis(3,4,5-trimethoxy-benzoyloxy)-propyl-diazepane derivatives thereof
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, (2008/06/13)
There is disclosed a process for the production of 1,4-bis-[3-(3,4,5-trimethoxybenzyloxy)-propyl]-diazepane which consists of first reacting 3-aminopropanol with acrylonitrile and subsequently reacting in aqueous solution with formaldehyde and hydrocyanic acid or with formaldehyde and an alkali cyanide in the presence of alkali hydrogen sulfite to form cyanomethyl-(2-cyano-ethyl)-(3-hydroxy-propyl)-amine; hydrogenating the thus obtained reaction product in the presence of a hydrogenating catalyst and ammonia to 1 (3-hydroxy-propyl)-1,4-diazepane and reacting the latter compound for example with 3-halogen propanol or with allyl alcohol and introducing two 3,4,5-trimethoxy-benzoyl groups into the thus obtained reaction product by esterification.
