908003-80-5 Usage
Uses
Used in Organic Synthesis:
(6,7-DIMETHOXY-1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER is used as a key intermediate in the synthesis of various organic compounds. Its unique structural features allow for the creation of a wide range of molecules with different properties and applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (6,7-DIMETHOXY-1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER is used as a building block for the development of pharmaceuticals. Its structural versatility enables the design and synthesis of novel drug candidates with potential therapeutic benefits.
Used in Pharmaceutical Development:
(6,7-DIMETHOXY-1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER is employed as a starting material for the creation of new pharmaceuticals. Its potential pharmacological properties make it a promising candidate for the development of drugs targeting various medical conditions.
Used in the Synthesis of Biologically Active Molecules:
(6,7-DIMETHOXY-1H-INDOL-3-YL)-ACETIC ACID METHYL ESTER is used as a precursor in the synthesis of biologically active molecules. Its structural features facilitate the development of compounds with potential applications in the fields of biology and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 908003-80-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,0,0 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 908003-80:
(8*9)+(7*0)+(6*8)+(5*0)+(4*0)+(3*3)+(2*8)+(1*0)=145
145 % 10 = 5
So 908003-80-5 is a valid CAS Registry Number.
908003-80-5Relevant articles and documents
Total synthesis of the alkaloid (±)-aspidophytine based on carbonyl ylide cycloaddition chemistry
Mejia-Oneto, Jose M.,Padwa, Albert
experimental part, p. 285 - 302 (2009/02/07)
The RhII-catalyzed cycloaddition cascade of an indolyl-substituted α-diazo imide was used for the total synthesis of the complex pentacyclic alkaloid (±)-aspidophytine. Treatment of the resulting dipolar cycloadduct with BF3·OEt
Application of the Rh(II) cyclization/cycloaddition cascade for the total synthesis of (±)-aspidophytine
Mejia-Oneto, Jose M.,Padwa, Albert
, p. 3275 - 3278 (2007/10/03)
A new strategy for the synthesis of (±)-aspidophytine has been developed and is based on a Rh(II)-catalyzed cyclization/dipolar cycloaddition sequence. The resulting [3+2]-cycloadduct undergoes an efficient Lewis acid mediated cascade that rapidly provide