2354-61-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Butanone, 1-(4-fluorophenyl)-4-(4-phenyl-1-piperazinyl)is used as an active pharmaceutical ingredient for the development of drugs targeting various medical conditions. Its unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for drug discovery and development.
Used in Chemical Research:
In the field of chemical research, 1-Butanone, 1-(4-fluorophenyl)-4-(4-phenyl-1-piperazinyl)can be used as a starting material or intermediate in the synthesis of more complex molecules. Its reactivity and functional groups make it a valuable compound for exploring new chemical reactions and developing novel chemical entities.
Used in Drug Delivery Systems:
Similar to gallotannin, 1-Butanone, 1-(4-fluorophenyl)-4-(4-phenyl-1-piperazinyl)can be employed in the development of drug delivery systems. Its chemical properties may allow for the creation of innovative carriers or enhancers for the delivery of therapeutic agents, potentially improving their bioavailability and efficacy.
Check Digit Verification of cas no
The CAS Registry Mumber 2354-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2354-61:
(6*2)+(5*3)+(4*5)+(3*4)+(2*6)+(1*1)=72
72 % 10 = 2
So 2354-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H23FN2O/c21-18-10-8-17(9-11-18)20(24)7-4-12-22-13-15-23(16-14-22)19-5-2-1-3-6-19/h1-3,5-6,8-11H,4,7,12-16H2
2354-61-2Relevant academic research and scientific papers
Piperazinobutyrophenone derivatives
-
, (2008/06/13)
Central nervous system active butyrophenone derivatives in which γ -piperazinobutyrophenone derivatives of the formula, SPC1 Wherein R1 is hydrogen, amino, C1 -C5 alkanoylamino, C1 -C4 alkylamino or N-(C1 -C4 alkyl)(C1 -C5 alkanoyl) amino; R2 is hydrogen or halogen; R3 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkoxy or trifluoromethyl; and m is 0, 1 or 2, and acid addition salts thereof, can be prepared by reacting an indole derivative of the formula, SPC2 Wherein R2, R3 and m are the same as defined above, and R4 and R5 are hydrogen or C1 -C4 alkyl respectively, with an oxidizing agent to yield an o-alkanoylamino-γ-piperazinobutyrophenone derivative of the formula, SPC3 Wherein R2, R3, R4, R5 and m are the same as defined above, and further, if necessary, hydrolyzing the product to yield an o-amino-γ-piperazinobutyrophenone derivative of the formula, SPC4 Wherein R2, R3, R5 and m are the same as defined above, and further diazotizing, if desired, in case R5 is hydrogen, the obtained o-amino-γ-piperazinobutyrophenone derivative and subsequently decomposing the resultant diazonium compound to replace the diazonium group by hydrogen. Among the butyrophenone derivatives thus obtained, those in which R1 is amino, alkanoylamino, alkylamino or N-alkylalkanoylamino and those in which R1 is hydrogen and R2 is halogen substituted at meta-position to carbonyl group are novel compounds.
