18903-05-4 Usage
Uses
Used in Pharmaceutical Industry:
1-HEXANOYL-PIPERAZINE is used as an intermediate for the synthesis of various pharmaceuticals, particularly for the development of antiviral and antibacterial drugs. Its chemical structure allows it to be a potential building block for creating new therapeutic agents, enhancing the range of treatments available in the medical field.
Used in Drug Delivery Systems:
1-HEXANOYL-PIPERAZINE is utilized in drug delivery systems to improve the efficacy and targeted delivery of pharmaceuticals. Its properties make it suitable for enhancing the bioavailability and therapeutic outcomes of drugs, contributing to more effective treatments.
Used in Chemical Industry:
1-HEXANOYL-PIPERAZINE has been studied for its potential use as an anticorrosive agent, indicating its application in protecting materials from corrosion and extending their lifespan. This makes it valuable in various industrial applications where corrosion resistance is crucial.
Used in Industrial Applications:
Beyond its pharmaceutical relevance, 1-HEXANOYL-PIPERAZINE also finds use in other industrial sectors, where its chemical properties can be harnessed for specific purposes, such as in the development of new materials or processes that benefit from its unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 18903-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18903-05:
(7*1)+(6*8)+(5*9)+(4*0)+(3*3)+(2*0)+(1*5)=114
114 % 10 = 4
So 18903-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2O/c1-2-3-4-5-10(13)12-8-6-11-7-9-12/h11H,2-9H2,1H3
18903-05-4Relevant articles and documents
Molecular simplification of 1,4-diazabicyclo[4.3.0]nonan-9-ones gives piperazine derivatives that maintain high nootropic activity
Manetti,Ghelardini,Bartolini,Dei,Galeotti,Gualtieri,Romanelli,Teodori
, p. 4499 - 4507 (2007/10/03)
Several 4-substituted 1-acylpiperazines, obtained by molecular simplification of 4-substituted 1,4-diazabicyclo[4.3.0]nonan-9-ones, have been synthesized and tested in vivo on the mouse passive avoidance test, to evaluate their nootropic activity. The results show that, apparently, an N-acylpiperazine group can mimic the 2-pyrrolidinone ring of 1,4-diazabicyclo[4.3.0]nonan-9-one, as the compounds of the new series maintain high nootropic activity. Moreover molecular simplification produces more clear-cut structure-activity relationships with respect to the parent series. The mechanism of action also appears to be similar in the two series. In fact, although the molecular mechanism remains to be elucidated, the most potent compound of each class (DM232 and 13, DM235) is able to increase acetylcholine release in rat brain. Piperazine derivatives represent a new class of nootropic drugs with an in vivo pharmacological profile very similar to that of piracetam, showing much higher potency with respect to the reference compound. Among the compounds studied, 13 (DM235) shows outstanding potency, being active at a dose of 0.001 mg kg-1 sc.
