91075-45-5 Usage
Explanation
This is the chemical name of the compound, which is a derivative of piperidine and a hydrochloride salt form.
Explanation
The compound is commonly used in the field of pharmacology, which is the study of drugs and their effects on living organisms.
Explanation
1-butyl-4,4-diphenylpiperidine hydrochloride acts as a stimulant to the central nervous system, which includes the brain and spinal cord.
Explanation
The compound has a long-lasting effect on the central nervous system, making it suitable for extended treatment periods.
Explanation
1-butyl-4,4-diphenylpiperidine hydrochloride does not have pain-relieving properties, which means it is not used to treat pain.
Explanation
The compound does not have properties that make it prone to abuse or addiction, which is an important consideration for its potential therapeutic use.
Explanation
1-butyl-4,4-diphenylpiperidine hydrochloride has been studied for its potential use in treating various neurological and psychiatric disorders, such as attention deficit hyperactivity disorder (ADHD) and Alzheimer's disease.
Explanation
The compound has been investigated as a potential treatment for substance abuse and addiction, which could make it a valuable addition to existing treatment options.
Explanation
Further research and clinical trials are needed to fully understand the potential therapeutic applications of 1-butyl-4,4-diphenylpiperidine hydrochloride, as its effects and safety profile are not yet fully established.
Field of use
Pharmacology
Type of compound
Central nervous system stimulant
Duration of action
Long-acting
Analgesic properties
Non-analgesic
Potential for abuse
Non-narcotic, non-addictive
Potential applications
Treating neurological and psychiatric disorders
Substance abuse treatment
Possible treatment option
Research status
Ongoing
Check Digit Verification of cas no
The CAS Registry Mumber 91075-45-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,7 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91075-45:
(7*9)+(6*1)+(5*0)+(4*7)+(3*5)+(2*4)+(1*5)=125
125 % 10 = 5
So 91075-45-5 is a valid CAS Registry Number.
91075-45-5Relevant academic research and scientific papers
Synthesis, physico-chemical properties and pharmacological screening results of budipine and related 1-alkyl-4,4-diphenylpiperidines
Schaefer,Hackmack,Eistetter,Krueger,Menge,Klosa
, p. 233 - 240 (2007/10/02)
1-Alkyl-4,4-diphenylpiperidines are accessible in a simple manner and with attractive yields by regioselective reaction of certain piperidine derivatives, particularly 3-aroyl-4-aryl-4-hydroxypiperidines, which can be varied widely at the nitrogen atom, with benzene under Friedel-Crafts conditions. The physico-chemical parameters, which are important for the transport and the distribution of a drug in a living system, are discussed for the 1-tert-butyl derivative (13) (budipine) (pK(a), partition coefficient P, saturation concentration c(s), surface activity, protein binding). Rapid absorption of this drug in man is indicated by the size of the permeability coefficient P(M) of the passive transport through artificial phospholipid collodium membranes as well as the invasion curves calculated from P(M). According to pharmacological screening tests, most of the compounds of this class show marked antagonistic activity against experimentally generated pathological states in mice (tremorine and reserpine antagonism) which suggest their potential use in the therapy of Parkinson's disease. 13 has been selected for detailed investigations. Structure-activity analyses did not readily demonstrate the presence of a relationship between the type of alkyl substituent at the piperidine nitrogen atom and the pharmacological screening results obtained.
4,4-Diarylpiperidine compositions and use
-
, (2008/06/13)
4,4-Diarylpiperidine compounds, preferably 4,4-diphenylpiperidine which are substituted or unsubstituted in the 1-position of the piperidine nucleus, such as 1-(lower alkyl)-4,4-diphenylpiperidines, 1-(lower alkyl)-4-phenyl-4-tolylpiperidines, and their s
4,4-Diarylpiperidines and process of making the same
-
, (2008/06/13)
4,4-Diarylpiperidine compounds, preferably 4,4-diphenylpiperidine which are substituted or unsubstituted in the 1-position of the piperidine nucleus, such as 1-(lower alkyl)-4,4-diphenylpiperidines, 1-(lower alkyl)-4-phenyl-4-tolylpiperidines, and their s
