184150-96-7 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-Methyl-1H-indole-6-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic benefits. Its unique chemical properties and biological activities make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
Methyl 2-Methyl-1H-indole-6-carboxylate is also utilized in the production of agrochemicals, contributing to the development of effective and innovative solutions for agricultural applications.
Used in Organic Synthesis:
Methyl 2-Methyl-1H-indole-6-carboxylate is employed as a key component in the synthesis of various organic compounds, showcasing its versatility and importance in organic chemistry.
Used in Research and Development:
Due to its unique chemical properties and potential applications across different industries, Methyl 2-Methyl-1H-indole-6-carboxylate is used in research and development laboratories to explore its capabilities and further its understanding in scientific and industrial contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 184150-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,1,5 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 184150-96:
(8*1)+(7*8)+(6*4)+(5*1)+(4*5)+(3*0)+(2*9)+(1*6)=137
137 % 10 = 7
So 184150-96-7 is a valid CAS Registry Number.
184150-96-7Relevant academic research and scientific papers
Intramolecular cyclization reactions of unsaturated amino Fischer chromium carbenes forming indoles and quinolines
S?derberg, Bj?rn C. G.,Shriver, James A.,Cooper, Seth H.,Shrout, Timothy L.,Helton, E. Scott,Austin, Lucinda R.,Odens, Herman H.,Hearn, Brian R.,Jones, Paula C.,Kouadio, Tiara N.,Ngi, Tan H.,Baswell, Rachel,Caprara, H. John,Meritt, Mark D.,Mai, Than T.
, p. 8775 - 8791 (2007/10/03)
A thermally induced intramolecular annulation reaction of N-(2-alkenylphenyl)amino substituted Fischer chromium carbenes has been extensively examined. The carbene complexes were prepared in moderate to good yields by reaction of 2-aminostyrenes with intermediately formed acyloxy substituted carbenes. Upon heating, the thermally labile carbenes decomposed producing indoles and quinolines as the major products. The product distribution was found to be highly dependent on the substitution pattern and electronic properties of the starting material, and on the solvent used.
Synthesis of 2,4-disubstituted indoles via thermal cyclization of N-trifluoroacetyl enehydrazines
Miyata, Okiko,Takeda, Norihiko,Naito, Takeaki
, p. 1101 - 1107 (2007/10/03)
Synthesis of naturally occurring indoles, 2,4-dimethylindole and 4-hydroxymethyl-2-methylindole by applying thermal cyclization of N-trifluoroacetyl enehydrazines is described.
