94012-35-8 Usage
Chemical classification
piperazine class of organic compounds
Derivative
a derivative of piperazine
Acetyl group attachment
contains an additional acetyl group attached to one of the nitrogen atoms
Pharmacological and therapeutic properties
studied for its potential pharmacological and therapeutic properties
Treatment potential
potential treatment for neurological and psychiatric disorders
Synthesis applications
investigated for its potential use in the synthesis of new pharmaceuticals and medicinal compounds
Research status
a relatively new and emerging chemical compound, requiring further research for understanding its potential uses and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 94012-35-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94012-35:
(7*9)+(6*4)+(5*0)+(4*1)+(3*2)+(2*3)+(1*5)=108
108 % 10 = 8
So 94012-35-8 is a valid CAS Registry Number.
94012-35-8Relevant academic research and scientific papers
Studies in Potential Filaricides: Part 20 - Synthesis of 1,4-Disubstituted Piperazines as Diethylcarbamazine Analogs
Charles, Elisabeth S.,Sharma, Satyavan
, p. 752 - 756 (2007/10/02)
A series of substituted 2,4-dimethylpiperazines (10-15), 1-benzyl-2-methylpiperazines (16-19), 1-substituted 3-methylpiperazines (20-25,27) and 1,4-disubstituted piperazines (28-34) have been synthesized starting from 1-benzyl-2-methylpiperazine (9) and 1
Studies in Potential Filaricides: Part XV - Synthesis of 1-Acyl/Aryl-4-substituted-piperazines as Diethylcarbamazine Analogs
Agrawal, V. K.,Sharma, Satyavan
, p. 650 - 654 (2007/10/02)
1-Acyl-4-substituted-piperazines (4-29) have been prepared starting from 1-benzylpiperazine while 1-aryl-4-aroylpiperazines (30-44) have been obtained from the corresponding 1-arylpiperazines.None of the compounds shows any significant filaricidal activity against Litomosoides carinii in cotton rats and cestodicial activity against Hymenolepis nana in mice.
