429689-18-9 Usage
Uses
Used in Pharmaceutical Industry:
(R)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is used as a building block for the synthesis of various organic compounds, which can be further utilized in the development of medications. Its unique structure and chiral properties make it a valuable component in the creation of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, (R)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is used as a key component in the synthesis of a range of organic compounds. Its versatility and structural complexity allow for the creation of diverse chemical products that can be applied in various fields, including materials science, agriculture, and environmental management.
Used in Research and Development:
(R)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE also serves as a valuable research tool in the study of organic chemistry and drug discovery. Its unique properties and potential applications make it an interesting subject for scientific investigation, contributing to the advancement of knowledge in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 429689-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,9,6,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 429689-18:
(8*4)+(7*2)+(6*9)+(5*6)+(4*8)+(3*9)+(2*1)+(1*8)=199
199 % 10 = 9
So 429689-18-9 is a valid CAS Registry Number.
429689-18-9Relevant academic research and scientific papers
Enantioselective friedel-crafts alkylations catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes
Evans, David A.,Fandrick, Keith R.,Song, Hyun-Ji,Scheidt, Karl A.,Xu, Risheng
, p. 10029 - 10041 (2008/03/12)
The enantioselective Friedel-Crafts addition of a variety of indoles catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes (Sc(III)-pybox) was accomplished utilizing a series of β-substituted α,β-unsaturated phosphonates and α,β-unsaturate
Enantioselective indole Friedel-Crafts alkylations catalyzed by bis(oxazolinyl)pyridine-scandium(III) triflate complexes
Evans, David A.,Scheidt, Karl A.,Fandrick, Keith R.,Lam, Hon Wai,Wu, Jimmy
, p. 10780 - 10781 (2007/10/03)
A highly enantioselective Friedel-Crafts alkylation of electron-rich aromatic nucleophiles catalyzed by scandium(III) triflate-pyridyl(bis)oxazoline complexes has been accomplished. The reaction involves α,β-unsaturated acyl phosphonates as electrophiles and primarily substituted indoles as nucleophiles. The reactive acyl phosphonate product is converted to the corresponding ester or amide in good overall yield by adding an alcohol or amine directly to the reaction mixture. Copyright
