149490-78-8 Usage
Uses
Used in Pharmaceutical Research and Drug Discovery:
4-BPIB is used as an enzyme and receptor inhibitor for [application reason] in the field of neuroscience. Its ability to modulate the release of neurotransmitters makes it a valuable tool for studying the central nervous system and contributes to the development of new therapeutic agents.
Used in Neuroscience Applications:
In the field of neuroscience, 4-BPIB is used as a research compound for [application reason] to investigate its potential in treating neurological disorders and understanding the mechanisms of neurotransmission.
Used in Anti-inflammatory Applications:
4-BPIB is used as an anti-inflammatory agent for [application reason] to alleviate inflammation and potentially treat conditions associated with inflammatory processes.
Used in Antitumor Applications:
In oncology, 4-BPIB is used as an antitumor agent for [application reason] to inhibit tumor growth and progression, offering a potential therapeutic strategy for cancer treatment.
Used in Alzheimer's Disease Research:
4-BPIB is used as a therapeutic agent for [application reason] in Alzheimer's disease research, exploring its potential to mitigate cognitive decline and neurodegeneration associated with the condition.
Used in Cancer Research and Treatment:
4-BPIB is used as a potential cancer treatment for [application reason] in cancer research, targeting specific enzymes and receptors that contribute to tumor development and growth.
Check Digit Verification of cas no
The CAS Registry Mumber 149490-78-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,4,9 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 149490-78:
(8*1)+(7*4)+(6*9)+(5*4)+(4*9)+(3*0)+(2*7)+(1*8)=168
168 % 10 = 8
So 149490-78-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13BrN2O/c14-12-5-3-11(4-6-12)13(17)2-1-8-16-9-7-15-10-16/h3-7,9-10H,1-2,8H2
149490-78-8Relevant academic research and scientific papers
Synthesis of 1-aryl-4-azolylbutanones
Karachev,Popkov
, p. 987 - 993 (2007/10/03)
A convenient method was developed for the synthesis of substituted 4-azolyl-1-arylbutanones from the available γ-chlorobutyrophenones by successive stages of transformation into ketals, alkylation of sodium imidazolate or 1,2,4-triazolate by the ketals in
Reaction of Aromatic Ketones with 3-Mercapto-1,2-propanediol. Synthesis of cis- and trans-2-Alkyl-2-aryl-(1,3-oxathiolane-5-methanols and 1,3-dioxolane-4-methanethiols)
Upadhyaya, Subhash,Bauer, Ludwig
, p. 1053 - 1065 (2007/10/02)
Aromatic ketones react with 3-mercapto-1,2-propanediol (1) in refluxing benzene under the catalytic influence of sulfonic acid and with azeotropic removal of water to yield a mixture comprised predominantly of cis- and trans-2-alkyl-2-aryl-1,3-oxathiolane
