40742-32-3 Usage
Description
3,4-Methylenedioxyphenylisobutylamine is an organic compound with a molecular structure that includes a phenyl ring with two methoxy groups at the 3 and 4 positions, and an isobutylamine side chain. It is related to certain psychoactive substances and has been a subject of interest in the field of pharmacology.
Uses
Used in Pharmaceutical Research:
3,4-Methylenedioxyphenylisobutylamine is used as a research compound for understanding its potential psychoactive effects and exploring its applications in the development of new medications. Its structural similarity to known psychoactive substances makes it a valuable tool in studying the mechanisms of action and potential therapeutic uses.
Used in Recreational Drug Studies:
Due to its relationship with 3,4-Methylenedioxyamphetamine/MDA, a recreational drug, 3,4-methylenedioxyphenylisobutylamine is used as a subject of study in the field of recreational drug research. This helps in understanding the effects of similar compounds on human health and behavior, and contributes to the development of harm reduction strategies and policies.
Please note that the use of 3,4-methylenedioxyphenylisobutylamine or any related compounds in recreational settings is not endorsed or recommended, as their safety and legal status may vary depending on the jurisdiction. The information provided is for educational purposes and to facilitate scientific understanding.
Check Digit Verification of cas no
The CAS Registry Mumber 40742-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,4 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40742-32:
(7*4)+(6*0)+(5*7)+(4*4)+(3*2)+(2*3)+(1*2)=93
93 % 10 = 3
So 40742-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-8(12)2-3-9-4-5-10-11(6-9)14-7-13-10/h4-6,8H,2-3,7,12H2,1H3
40742-32-3Relevant articles and documents
CATALYST COMPOUNDS
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Paragraph 0314; 0322, (2015/03/28)
The present invention relates to an iridium-based catalyst compound for hydrogenating reducible moieties, especially imines and iminiums, the catalyst compounds being defined by the formulas: where ring B is either itself polycyclic, or ring B together with R is polycyclic. The catalysts of the invention are particularly effective in reductive amination procedures 10 which involve the in situ generation of the imine or iminium under reductive hydrogenative conditions.
CATALYST COMPOUNDS
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Paragraph 00163; 00171, (2013/11/05)
The present invention relates to an iridium-based catalyst compound for hydrogenating reducible moieties, especially imines and iminiums, the catalyst compounds being defined by the formulas: where ring B is either itself polycyclic, or ring B together with R is polycyclic. The catalysts of the invention are particularly effective in reductive amination procedures 10 which involve the in situ generation of the imine or iminium under reductive hydrogenative conditions.
Hydrogenolysis of 3-methyl-4-phenylmethyl-5(2H)-isoxazolone derivatives: A reinvestigation
Batra, Sanjay,Seth, M,Bhaduri, A P
, p. 60 - 62 (2007/10/02)
Hydrogenolysis of 3-methyl-4-phenylmethyl-5(2H)-isoxazolone (2a) and its derivatives 2b-e, 5a-e, 6a-e and 9a,b have been carried out over Pd/C and Raney-nickel.The products have been isolated and characterized.The intermediate products of hydrogenolysis of 2b-e have been trapped and simultaneous cleavage of N - O and C - C bonds in 9a,b has been suggested to explain the formation of the hydrogenolysis products 10a,b and 3a,b.
