41787-64-8 Usage
Description
1-(3,4-dimethoxyphenyl)-2-methylamino-ethanol is a compound that is a metabolite of phenethylamine drugs. It is typically isolated from the Dona Ana cactus and possesses psychoactive properties similar to those of Mescaline or Psilocin.
Uses
Used in Pharmaceutical Industry:
1-(3,4-dimethoxyphenyl)-2-methylamino-ethanol is used as a psychoactive compound for its ability to produce effects similar to Mescaline or Psilocin. Its potential applications in the pharmaceutical industry may include the development of new treatments for various conditions related to mood and mental health.
Used in Research and Development:
As a metabolite of phenethylamine drugs, 1-(3,4-dimethoxyphenyl)-2-methylamino-ethanol can be used in research and development for understanding the mechanisms of action and potential therapeutic applications of psychoactive substances. This knowledge can contribute to the development of new drugs and therapies for various neurological and psychiatric disorders.
Used in Ethnopharmacology:
1-(3,4-dimethoxyphenyl)-2-methylamino-ethanol is used as a component in the study of traditional and indigenous medicinal practices. Its presence in the Dona Ana cactus and its psychoactive properties make it an interesting subject for ethnopharmacological research, which aims to explore the cultural and medicinal significance of such plants and their compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 41787-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41787-64:
(7*4)+(6*1)+(5*7)+(4*8)+(3*7)+(2*6)+(1*4)=138
138 % 10 = 8
So 41787-64-8 is a valid CAS Registry Number.
41787-64-8Relevant articles and documents
An in situ procedure for catalytic, enantioselective acetate aldol addition. Application to the synthesis of (R)-(-)-epinephrine
Singer, Robert A.,Carreira, Erick M.
, p. 927 - 930 (2007/10/03)
We report an in situ preparation of catalyst 3 which substantially simplifies the experimental procedure for the enantioselective, catalytic acetate aldol addition reaction. The addition of Me3SiCl and Et3N circumvents the azeotropic removal of the released isopropanol upon treating ligands 1 and 2 with Ti(O(i)Pr)4. Importantly, this new procedure maintains the salient features of the catalytic process we originally described: high yields and enantioselectivities, low catalyst loads, and convenient reaction times and temperatures. We have applied the new procedure to an efficient synthesis of (R)-(-)-epinephrine from commercially available reagents in an overall yield of 45%.
