78551-90-3 Usage
Classification
Psychoactive compound, piperazine derivative
Usage
Recreational drug
Effects
Stimulant effects, similar to amphetamines
Mechanism of Action
Acts on the central nervous system, increasing the release of serotonin and dopamine
Resulting Feelings
Euphoria, heightened energy levels
Popularity
Often used as a party drug
Side Effects
Nausea, anxiety, insomnia
Legal Status
Illegal in many countries, categorized as a controlled substance
Potential Issues
Abuse and dependence risks
Check Digit Verification of cas no
The CAS Registry Mumber 78551-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,5 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78551-90:
(7*7)+(6*8)+(5*5)+(4*5)+(3*1)+(2*9)+(1*0)=163
163 % 10 = 3
So 78551-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H24N2/c1-13(2)10-15-11-16-8-9-17(15)12-14-6-4-3-5-7-14/h3-7,13,15-16H,8-12H2,1-2H3/t15-/m0/s1
78551-90-3Relevant academic research and scientific papers
Synthesis and structure of 1,4-dipiperazino benzenes: Chiral terphenyl-type peptide helix mimetics
Maity, Prantik,Koenig, Burkhard
supporting information; experimental part, p. 1473 - 1476 (2009/04/10)
(Chemical Equation Presented) The terphenyl structure has been proven to be an ideal scaffold mimicking side-chain functionalities of peptidic α-helices. The synthesis of 1,4-dipiperazino benzenes, using stepwise transition metal-catalyzed N-arylation of chiral piperazines to a central benzene core is reported. The structure determination by X-ray crystallography reveals a geometrical arrangement of the hydrophobic side chains resembling the orientation of key i, i + 3, and i + 7 positions in a peptidic α-helix or in terphenyl helix mimetics.
Piperazinone and piperazine polypeptides
-
, (2008/06/13)
Piperazinone polypeptides which are useful as analgesics and psychotherapeutic agents as well as processes to produce them are described.
