156333-97-0 Usage
Uses
Used in Pharmaceutical Drug Synthesis:
1-(2-IODOBENZYL)-4-METHYLPIPERAZINE is used as a building block for the synthesis of various pharmaceutical drugs and research chemicals. Its iodobenzyl group allows for further functionalization, which is crucial for the development of new drugs with specific therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1-(2-IODOBENZYL)-4-METHYLPIPERAZINE is used as a versatile compound for research purposes. Its ability to be modified with additional chemical groups makes it a valuable tool for exploring new drug candidates and understanding their mechanisms of action.
Used in Drug Development:
1-(2-IODOBENZYL)-4-METHYLPIPERAZINE is also used in drug development due to its flexibility and solubility provided by the 4-methylpiperazine moiety. These characteristics are essential for enhancing the compound's bioavailability and overall effectiveness in potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 156333-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,3,3 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 156333-97:
(8*1)+(7*5)+(6*6)+(5*3)+(4*3)+(3*3)+(2*9)+(1*7)=140
140 % 10 = 0
So 156333-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17IN2/c1-14-6-8-15(9-7-14)10-11-4-2-3-5-12(11)13/h2-5H,6-10H2,1H3
156333-97-0Relevant academic research and scientific papers
ALKYNYL PHOSPHINE GOLD COMPLEXES FOR TREATING BACTERIAL INFECTIONS
-
Page/Page column 85, (2017/08/01)
A compound of formula (I) for use in the prevention or treatment of a bacterial infection.
An approach to α-substituted amines
Williams, Lorenzo,Booth, Susan E.,Undheim, Kjell
, p. 13697 - 13708 (2007/10/02)
A number of amines have been alkylated at the position alpha to nitrogen via free radical methodology. N-(2-iodobenzyl) and N-(2-iodobenzoyl) 'protected' amines have been used to generate radicals which rapidly undergo a 1,5-hydrogen shift to give more st
α-Alkylation of Amines via a 1,5-Hydrogen Shift
Undheim, Kjell,Williams, Lorenzo
, p. 883 - 884 (2007/10/02)
Radicals derived from N-(2-iodobenzyl) 'protected' amines undergo a 1,5-hydrogen shift to give more stable α-amino radicals, which can be subsequently trapped by electron deficient alkenes.
