90389-89-2 Usage
Uses
Used in Pharmaceutical Industry:
N-(3-CHLOROBENZYL)-N-ISOPROPYLAMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, N-(3-CHLOROBENZYL)-N-ISOPROPYLAMINE serves as an intermediate in the production of agrochemicals. Its properties make it suitable for the creation of compounds that can be used in agriculture to protect crops and enhance yields.
Used in Organic Synthesis:
N-(3-CHLOROBENZYL)-N-ISOPROPYLAMINE is utilized as a reagent in organic synthesis, facilitating various chemical reactions. Its presence can help in the formation of complex organic molecules, which are essential in a wide range of applications.
Used in Chemical Research:
As a valuable chemical in the field of organic chemistry, N-(3-CHLOROBENZYL)-N-ISOPROPYLAMINE is employed in chemical research to explore new reactions, mechanisms, and the development of innovative synthetic methods. Its unique properties make it a useful tool for scientists in understanding and advancing chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 90389-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,8 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90389-89:
(7*9)+(6*0)+(5*3)+(4*8)+(3*9)+(2*8)+(1*9)=162
162 % 10 = 2
So 90389-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14ClN/c1-8(2)12-7-9-4-3-5-10(11)6-9/h3-6,8,12H,7H2,1-2H3
90389-89-2Relevant academic research and scientific papers
Transformation of N,N-diisopropylarylmethylamines into N-isopropylarylmethylamines with molecular iodine
Ezawa, Masatoshi,Moriyama, Katsuhiko,Togo, Hideo
, p. 6689 - 6692 (2016/02/03)
N,N-Diisopropylarylmethylamines were smoothly converted into the corresponding N-isopropylarylmethylamines by the reaction with molecular iodine in the presence of Na2CO3 in chloroform at 60 °C. Other related tertiary amines were also transformed into the corresponding secondary amines by the reaction with molecular iodine under the same reaction conditions.
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.
