807342-83-2 Usage
General Description
N-(3,4-dimethoxybenzyl)propylamine is a chemical compound with the molecular formula C12H19NO2. It is a substituted phenethylamine that consists of a propylamine bound to the benzyl group, which is in turn substituted by methoxy groups at the 3 and 4 positions. N-(3,4-dimethoxybenzyl)propylamine has a variety of potential applications, including as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It may also be used as a reagent in chemical research and synthesis, and it has the potential to exhibit biological activity that could make it useful in medicinal chemistry. Due to its potential for interacting with biological systems and its structural similarity to other biologically active compounds, N-(3,4-dimethoxybenzyl)propylamine may possess a range of pharmacological properties that could be of interest for further study.
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 articles and documents
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
