62924-69-0 Usage
Uses
Used in Pharmaceutical Synthesis:
[(2,6-dichlorophenyl)methyl](propyl)amine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of diverse medicinal compounds, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
[(2,6-dichlorophenyl)methyl](propyl)amine also serves as an essential building block in the production of agrochemicals. Its incorporation into the chemical structure of agrochemicals can enhance their effectiveness in pest control, crop protection, and other agricultural applications.
Used in Coordination Chemistry:
[(2,6-dichlorophenyl)methyl](propyl)amine has been studied for its potential as a ligand in coordination chemistry. Its ability to form stable complexes with metal ions can lead to the development of new materials with specific properties, such as catalysts, sensors, or materials with unique electronic or magnetic characteristics.
Used in Chemical Engineering:
[(2,6-dichlorophenyl)methyl](propyl)amine's structure and properties make it valuable in various fields of chemical engineering. It can be utilized in the design and synthesis of advanced materials, polymers, and other chemical products, further expanding its applications in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 62924-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,2 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62924-69:
(7*6)+(6*2)+(5*9)+(4*2)+(3*4)+(2*6)+(1*9)=140
140 % 10 = 0
So 62924-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H13Cl2N/c1-2-6-13-7-8-9(11)4-3-5-10(8)12/h3-5,13H,2,6-7H2,1H3
62924-69-0Relevant academic research and scientific papers
Benzylamines: Synthesis and evaluation of antimycobacterial properties
Meindl,Von Angerer,Schonenberger,Ruckdeschel
, p. 1111 - 1118 (2007/10/02)
The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.
