807342-83-2 Usage
Uses
Used in Pharmaceutical Industry:
N-(3,4-dimethoxybenzyl)propylamine is used as a precursor in the synthesis of pharmaceuticals for its potential to contribute to the development of new drugs with various therapeutic applications.
Used in Agrochemical Industry:
N-(3,4-dimethoxybenzyl)propylamine is used as a precursor in the synthesis of agrochemicals to aid in the creation of compounds that can enhance crop protection and yield.
Used in Chemical Research and Synthesis:
N-(3,4-dimethoxybenzyl)propylamine is used as a reagent in chemical research and synthesis, facilitating the exploration of new chemical reactions and the development of novel organic compounds.
Used in Medicinal Chemistry:
N-(3,4-dimethoxybenzyl)propylamine is used in medicinal chemistry for its potential biological activity, which may lead to the discovery of new pharmacological properties and applications in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 807342-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,7,3,4 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 807342-83:
(8*8)+(7*0)+(6*7)+(5*3)+(4*4)+(3*2)+(2*8)+(1*3)=162
162 % 10 = 2
So 807342-83-2 is a valid CAS Registry Number.
807342-83-2Relevant academic research and scientific papers
Preparation of benzolactams by Pd(OAC)2-catalyzed direct aromatic carbonylation
Orito, Kazuhiko,Horibata, Akiyoshi,Nakamura, Takatoshi,Ushito, Harumi,Nagasaki, Hideo,Yuguchi, Motoki,Yamashita, Satoshi,Tokuda, Masao
, p. 14342 - 14343 (2007/10/03)
We developed a new method for Pd(II)-catalyzed direct aromatic carbonylation in a phosphine-free catalytic system using Pd(OAc)2 and Cu(OAc)2 in an atmosphere of CO gas containing air. The carbonylation proceeded with ortho-palladation, inducing a remarkable site selectivity to afford a variety of five- or six-membered benzolactams from secondary ω-arylalkylamines, such as N-alkylbenzylamines or N-alkylphenethylamines. Copyright
