66264-86-6 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-METHYL 3-(P-METHOXYPHENYL)-PROPYLAMINE is used as an intermediate in the synthesis of various pharmaceuticals for its potential applications in the treatment of neurological disorders.
Used in Organic Synthesis:
(S)-1-METHYL 3-(P-METHOXYPHENYL)-PROPYLAMINE is used as a building block for the production of other important chemicals, contributing to the development of new organic compounds.
Used in Research and Industrial Processes:
(S)-1-METHYL 3-(P-METHOXYPHENYL)-PROPYLAMINE is used as a chemical reagent in various research and industrial processes, supporting the advancement of scientific knowledge and the creation of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 66264-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66264-86:
(7*6)+(6*6)+(5*2)+(4*6)+(3*4)+(2*8)+(1*6)=146
146 % 10 = 6
So 66264-86-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO/c1-9(12)3-4-10-5-7-11(13-2)8-6-10/h5-9H,3-4,12H2,1-2H3/t9-/m0/s1
66264-86-6Relevant academic research and scientific papers
Ir(I)-catalyzed enantioselective secondary sp3 C-H bond activation of 2-(alkylamino)pyridines with alkenes
Pan, Shiguang,Endo, Kohei,Shibata, Takanori
supporting information; experimental part, p. 4692 - 4695 (2011/11/06)
A cationic Ir(I)-tolBINAP complex catalyzed an enantioselective C-C bond formation initiated by secondary sp3 C-H bond cleavage adjacent to a nitrogen atom. The reaction of 2-(alkylamino)pyridines with various alkenes gave chiral amines in good yields with high enantiomeric excesses.
Betuligenol derivative with growth inhibition and antifeedant activity
Chattopadhyay, Sunil K.,Srivastava, Sachin,Sashidhara, Koneni V.,Tripathi, Arun K.,Bhattacharya, Asish K.,Negi, Arvind S.
, p. 1729 - 1731 (2007/10/03)
The title chiral amine, 3-(4-methoxyphenyl)-1-methylpropylamine 5 has been synthesized from naturally abundant betuligenol 1 in three steps and also in good yield. Furthermore, the versatile intermediate 3 could be manipulated for the preparation of chiral disulphide 7. The amine derivative 5 prepared from (-)-betuligenol showed significant growth inhibition and antifeedant activity.
