76464-88-5 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-IODOBENZYL)PIPERIDINE is used as an intermediate for the synthesis of various pharmaceuticals and organic compounds, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Industry:
1-(2-IODOBENZYL)PIPERIDINE is used as a versatile chemical in the chemical industry, playing a crucial role in the synthesis and production of different organic compounds.
Used in Research and Development:
1-(2-IODOBENZYL)PIPERIDINE is employed as a key compound in the research and development of new drugs, thanks to its potential pharmacological activities and biological properties.
Used in Anti-Inflammatory and Analgesic Applications:
1-(2-IODOBENZYL)PIPERIDINE is studied for its potential as an anti-inflammatory and analgesic agent, which could lead to the development of new treatments for pain and inflammation-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 76464-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,6 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76464-88:
(7*7)+(6*6)+(5*4)+(4*6)+(3*4)+(2*8)+(1*8)=165
165 % 10 = 5
So 76464-88-5 is a valid CAS Registry Number.
76464-88-5Relevant academic research and scientific papers
High-yielding synthesis of 1-isoindolinone derivatives via palladium-catalysed cycloaminocarbonylation
Marosv?lgyi-Haskó, Diána,Takács, Attila,Riedl, Zsuzsanna,Kollár, László
experimental part, p. 1036 - 1040 (2011/03/19)
1-Isoindolinone derivatives were synthesised in high yields (up to 89%) by using 2-iodobenzyl bromide and 2-iodobenzylamine as bifunctional substrates in palladium-catalysed carbonylation. Depending on the N-nucleophiles, two types of compounds were synth
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.
