57184-27-7 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(2-METHYL-ALLYL)-PIPERAZINE is used as a building block for the production of various drugs, contributing to the development of novel pharmaceuticals with improved efficacy and safety profiles.
Used in Biochemical Research:
In the field of biochemical research, 1-(2-METHYL-ALLYL)-PIPERAZINE serves as a valuable compound for studying the interactions and mechanisms of biological systems, potentially leading to the discovery of new therapeutic targets and treatments.
Used in Organic Chemistry:
1-(2-METHYL-ALLYL)-PIPERAZINE is utilized as a key component in organic chemistry, where its unique structure and properties facilitate the creation of new organic compounds with diverse applications.
Used in Medicinal Chemistry:
In medicinal chemistry, 1-(2-METHYL-ALLYL)-PIPERAZINE is employed as a ligand in coordination chemistry, playing a crucial role in the design and synthesis of complex molecular structures with potential therapeutic applications.
Used in Drug Discovery:
1-(2-METHYL-ALLYL)-PIPERAZINE is also used in drug discovery processes, where its structure and properties aid in the identification and development of new drugs with enhanced biological activity and potential therapeutic benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 57184-27-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,8 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57184-27:
(7*5)+(6*7)+(5*1)+(4*8)+(3*4)+(2*2)+(1*7)=137
137 % 10 = 7
So 57184-27-7 is a valid CAS Registry Number.
57184-27-7Relevant academic research and scientific papers
Unique spirocyclopiperazinium salt I: Synthesis and structure-activity relationship of spirocyclopiperazinium salts as analgesics
Gao, Feng-Li,Wang, Xin,Zhang, Hong-Mei,Cheng, Tie-Ming,Li, Run-Tao
, p. 1535 - 1537 (2007/10/03)
Based on the structure of compound 3, two series of spirocyclopiperazinium derivatives 7a-n and 10a-h were synthesized and evaluated for their in vivo analgesic and sedative activities. Compounds 7f and 10c were discovered to exhibit excellent analgesic activity. Structure-activity relationships revealed that anion of the quaternary salt affected the analgesic and sedative activity significantly; the allyl group is a most effective group among the compounds 7a-n; the electron-released substitute on the aromatic ring is favorable to increase the analgesic activity.
Naphthyridine derivatives
-
, (2008/06/13)
Compounds of the formula: STR1 wherein one of the symbols =X-- represents =N-- and the other three each represent a group STR2 in which Y represents hydrogen, halogen, alkyl, alkoxy, cyano or nitro, at least two of the symbols representing hydrogen, Z represents hydrogen, halogen, alkyl, alkoxy, trifluoromethyl or nitro, and (i) n represents zero and R represents hydrogen, alkyl, alkenyl, alkynyl, hydroxyalkyl or phenyl, or (ii) n represents 1 and R represents alkyl, hydroxyalkyl or phenyl, are new compounds possessing pharmacological properties; they are particularly active as tranquilizers and anti-convulsant agents.
