185678-56-2 Usage
Chemical compound
1-Indan-1-yl-piperazine is a chemical compound belonging to the class of piperazine derivatives.
Structure
It has a structure consisting of a piperazine ring attached to an indane group.
Central nervous system effects
It has been studied for its potential effects on the central nervous system.
Potential psychostimulant
1-Indan-1-yl-piperazine has been identified as a potential psychostimulant and has been investigated as a recreational drug.
Therapeutic applications
It has potential therapeutic applications, including its potential use as an antidepressant or in the treatment of neurological disorders.
Pharmacological properties
1-Indan-1-yl-piperazine has been the subject of research for its pharmacological properties and potential medical uses.
Check Digit Verification of cas no
The CAS Registry Mumber 185678-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,6,7 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 185678-56:
(8*1)+(7*8)+(6*5)+(5*6)+(4*7)+(3*8)+(2*5)+(1*6)=192
192 % 10 = 2
So 185678-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2/c1-2-4-12-11(3-1)5-6-13(12)15-9-7-14-8-10-15/h1-4,13-14H,5-10H2
185678-56-2Relevant articles and documents
NOVEL SUBSTITUTED PIPERAZINE AMIDE COMPOUNDS AS INDOLEAMINE 2, 3-DIOXYGENASE (IDO) INHIBITORS
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Page/Page column 198, (2020/06/19)
Disclosed herein are compounds of formula (I) which are inhibitors of an IDO enzyme: (I). Also disclosed herein are uses of the compounds in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising these compounds. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.
MELATONERGIC INDANYL PIPERAZINES
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, (2008/06/13)
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Synthesis of 1-[ω-[(arylamino)carbonyl]alkyl]-4-(benzocycloalkyl)piperazines
El-Ahmad, Youssef,Maillet, Philippe,Laurent, Elisabeth,Talab, Akram,Tran, Gilles,Ollivier, Roland
, p. 723 - 734 (2007/10/03)
A series of 1-[co-[(arylamino)carbonyl]alkyl]-4-(benzocycloalkyl)-piperazines (1a-v) was prepared either by reacting the precursor 4-[ω-[(arylamino)carbonyl]alkyl]piperazine (2a-j) with 1-chlorobenzocycloalkanes (3a-c) (Procedure A) or by reacting the N-aryl-ω-chloroalkanamides (5a-j) with the 4-(benzocycloalkyl)piperazines (10a-c) (Procedure B). The best yields were obtained using procedure A.
