18940-58-4 Usage
Uses
Used in Pharmaceutical Industry:
1,4-Diisobutyrylpiperazine is used as a reactant for the synthetic preparation of chloro enamines and bromo enamines, which are important intermediates in the synthesis of various pharmaceutical compounds. These enamines are key building blocks for the development of new drugs with potential applications in treating a wide range of medical conditions.
1,4-Diisobutyrylpiperazine is also used as a potential analgesic agent for the development of pain-relieving medications. Its investigation in this area highlights the compound's potential to contribute to the creation of new and effective pain management solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 18940-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18940-58:
(7*1)+(6*8)+(5*9)+(4*4)+(3*0)+(2*5)+(1*8)=134
134 % 10 = 4
So 18940-58-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H22N2O2/c1-9(2)11(15)13-5-7-14(8-6-13)12(16)10(3)4/h9-10H,5-8H2,1-4H3
18940-58-4Relevant academic research and scientific papers
Ryu, Ilhyong,Nagahara, Kiyoto,Kambe, Nobuaki,Sonoda, Noboru,Kreimerman, Sergio,Komatsu, Mitsuo
, p. 1953 - 1954 (1998)
Amides can be synthesized from alkyl iodides and amines in the presence of CO (20-25 atm), without using transition metal catalyst; the radical cascade is initiated thermally using AIBN and allyltributyltin.
A general and practical method of synthesis of 2-disubstituted-1- chloro- and 1-bromoenamines
Ghosez, Leon,George-Koch, Isabelle,Patiny, Luc,Houtekie, Marc,Bovy, Philippe,Nshimyumukiza, Prosper,Phan, Thao
, p. 9207 - 9222 (2007/10/03)
Disubstituted-α-chloroenamines are useful synthetic intermediates which had earlier been prepared by the reaction of tertiary amides with phosgene. The toxicity of the latter led us to systematically investigate new synthetic routes towards α-chloro- and