438245-97-7 Usage
Description
Benzenemethanamine, 3-methoxy-N,alpha-dimethyl(9CI), also known as 3-Methoxy-N,alpha-dimethylphenethylamine, is a psychoactive chemical compound belonging to the phenethylamine class. It possesses a molecular formula of C11H17NO and exhibits stimulant and entactogenic effects due to its structural resemblance to methamphetamine.
Uses
Used in Pharmaceutical Industry:
Benzenemethanamine, 3-methoxy-N,alpha-dimethyl(9CI) is used as a research chemical for the development of new medications and therapies. Its psychoactive properties make it a valuable compound for studying the effects of stimulants and entactogens on the human brain and nervous system.
Used in Forensic Science:
Benzenemethanamine, 3-methoxy-N,alpha-dimethyl(9CI) is utilized in forensic science for the identification and analysis of controlled substances in cases involving drug abuse and addiction. Its unique chemical structure allows for accurate detection and differentiation from other similar compounds.
Used in Recreational Settings:
Although it is considered a controlled substance in many countries, Benzenemethanamine, 3-methoxy-N,alpha-dimethyl(9CI) has been used recreationally for its psychoactive properties, providing users with stimulant and entactogenic effects. However, its potential for abuse and addiction makes it a substance that requires strict regulation and control.
Check Digit Verification of cas no
The CAS Registry Mumber 438245-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,2,4 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 438245-97:
(8*4)+(7*3)+(6*8)+(5*2)+(4*4)+(3*5)+(2*9)+(1*7)=167
167 % 10 = 7
So 438245-97-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c1-8(11-2)9-5-4-6-10(7-9)12-3/h4-8,11H,1-3H3
438245-97-7Relevant articles and documents
Oxidation Under Reductive Conditions: From Benzylic Ethers to Acetals with Perfect Atom-Economy by Titanocene(III) Catalysis
Funk, Pierre,Richrath, Ruben B.,Bohle, Fabian,Grimme, Stefan,Gans?uer, Andreas
, p. 5482 - 5488 (2021/02/03)
Described here is a titanocene-catalyzed reaction for the synthesis of acetals and hemiaminals from benzylic ethers and benzylic amines, respectively, with pendant epoxides. The reaction proceeds by catalysis in single-electron steps. The oxidative addition comprises an epoxide opening. An H-atom transfer, to generate a benzylic radical, serves as a radical translocation step, and an organometallic oxygen rebound as a reductive elimination. The reaction mechanism was studied by high-level dispersion corrected hybrid functional DFT with implicit solvation. The low-energy conformational space was searched by the efficient CREST program. The stereoselectivity was deduced from the lowest lying benzylic radical structures and their conformations are controlled by hyperconjugative interactions and steric interactions between the titanocene catalyst and the aryl groups of the substrate. An interesting mechanistic aspect is that the oxidation of the benzylic center occurs under reducing conditions.
Isoquinolines as IGF-1R Inhibitors
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Page/Page column 14, (2009/04/24)
Compounds of the formula (I): were synthesized. In at least one embodiment, they were found to down-regulate or inhibit the expression or function of the IGF-1 receptor.
ISOQUINOLINES AS IGF-1R INHIBITORS
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Page/Page column 50, (2010/11/26)
Compounds of the formula (I) were synthesized. They were found to down- regulate or inhibit the expression or function of the IGF-I receptor.
