17419-71-5 Usage
Chemical class
Piperazine derivatives
Explanation
1-phenyl-4-[(4-phenylpiperazin-1-yl)methyl]piperazine belongs to the class of piperazine derivatives, which are organic compounds commonly used in pharmaceutical drugs and research chemicals.
Explanation
The compound has a central piperazine ring structure with multiple phenyl (aromatic hydrocarbon) groups attached to it, contributing to its complexity.
Explanation
1-phenyl-4-[(4-phenylpiperazin-1-yl)methyl]piperazine has the potential to modify the activity of neurotransmitters in the brain, particularly serotonin and dopamine, which are responsible for mood regulation, motivation, and other cognitive functions.
Explanation
Due to its ability to modify neurotransmitter activity, the compound may be studied for its potential use in treating various neurological and psychiatric disorders, such as depression, anxiety, and schizophrenia.
Molecular structure
Piperazine core with multiple phenyl groups
Pharmacological properties
Modification of neurotransmitter activity
Potential applications
Treatment of neurological and psychiatric disorders
Check Digit Verification of cas no
The CAS Registry Mumber 17419-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17419-71:
(7*1)+(6*7)+(5*4)+(4*1)+(3*9)+(2*7)+(1*1)=115
115 % 10 = 5
So 17419-71-5 is a valid CAS Registry Number.
17419-71-5Relevant articles and documents
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Butler
, p. 482 (1956)
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Synthesis, characterization, and anti-amoebic screening of core-modified 5,20-bis{2-{[(alkyl)(alkyl′)amino]methyl}ferrocen-1-yl}-10,15-diphenyl-21, 23-dithiaporphyrin (=1,1″-(10,15-diphenyl-21,23-dithiaporphine-5,20-diyl) bis[2-{[(alkyl)(alkyl′)amino]methyl}ferrocene]) derivatives
Bhat, Abdul R.,Bhat, Asif I.,Athar, Fareeda,Azam, Amir
experimental part, p. 1644 - 1656 (2009/10/16)
The synthesis of the first bis-ferrocenyl-substituted core-modified porphyrins, 5,20-bis{2-{[(alkyl)-(alkyl′)amino]methyl}ferrocen-1-yl}-10, 15-diphenyl-21,23-dithiaporphyrin derivatives 6a - 6j, via a multistep route is reported (Schemes 1, 2, and 4). The synthesis was carried out through acid-catalyzed (BF3 ? Et2O) condensation of 1,1″- [thiophene-2,5-diylbis(hydroxymethyl)]bis[2-{[(alkyl)(alkyl′)amino]methyl} ferrocenes] 4a - 4j with 2,2′-[thiophene-2,5-diylbis(phenylmethylene)] bis[1H-pyrrole] (5b) in presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (=4,5-dichloro-3,6-dioxocyclohexa-1,4-diene-1,2-dicarbonitrile; DDQ). Characterization of the compounds was done at each step by means of various spectroscopic techniques. The final compounds were screened for in vitro anti-amoebic activity against the strain HM1:IMSS of E. histolytica (Table 2).
Synthesis and antimicrobial activity in vitro of N-substituted derivatives of phenylpiperidine and phenylpiperazine
Morlacchi,Trapani,Losacco,Armenise
, p. 671 - 682 (2007/10/02)
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