429689-17-8 Usage
Description
(S)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is a chemical compound that belongs to the class of phenylpropionates. It is a derivative of indole and phenylpropionic acid, characterized by a methyl group attached to the indole ring and a propionate ester at the phenyl ring. This structure confers specific chemical and biological properties, making it a valuable compound in the fields of organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
(S)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique structural features and potential pharmacological activities.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE serves as a versatile building block for the creation of more complex molecules, contributing to the development of novel chemical entities.
Used in Drug Development:
(S)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is used as a starting material for the development of new drugs, particularly those with potential analgesic or anti-inflammatory properties, thanks to its specific chemical and biological characteristics.
Used in Medicinal Chemistry:
In medicinal chemistry, (S)-METHYL-3-(1-METHYL-1H-INDOL-3-YL)-PHENYL-PROPIONATE is utilized for the design and optimization of drug candidates, taking advantage of its structural diversity and pharmacological potential to create effective therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 429689-17-8 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 429689-17:
(8*4)+(7*2)+(6*9)+(5*6)+(4*8)+(3*9)+(2*1)+(1*7)=198
198 % 10 = 8
So 429689-17-8 is a valid CAS Registry Number.
429689-17-8Relevant articles and documents
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
