36779-17-6 Usage
Description
Methyl 2-phenyl-1H-indole-3-carboxylate is a chemical compound with the molecular formula C17H15NO2. It is a methyl ester derivative of 2-phenyl-1H-indole-3-carboxylic acid and belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. Its structure consists of a phenyl group, a carboxylic acid ester group, and an indole ring, which gives it its characteristic odor and chemical properties. Methyl 2-phenyl-1H-indole-3-carboxylate is a valuable building block for the creation of diverse chemical compounds.
Uses
Used in Pharmaceutical Synthesis:
Methyl 2-phenyl-1H-indole-3-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its unique chemical properties and reactivity. It plays a crucial role in the development of new drugs and medicines.
Used in Perfume and Fragrance Production:
Methyl 2-phenyl-1H-indole-3-carboxylate is used as a key ingredient in the production of perfumes and fragrances due to its characteristic odor. It contributes to the creation of unique and complex scents in various fragrance formulations.
Used in Chemical Research:
Methyl 2-phenyl-1H-indole-3-carboxylate is used as a valuable building block in chemical research for the development of new compounds and materials. Its unique structure and properties make it an important tool for exploring new chemical reactions and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 36779-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,7 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36779-17:
(7*3)+(6*6)+(5*7)+(4*7)+(3*9)+(2*1)+(1*7)=156
156 % 10 = 6
So 36779-17-6 is a valid CAS Registry Number.
36779-17-6Relevant articles and documents
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Kitamura,R. et al.
, p. 2911 - 2914 (1977)
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Copper-Mediated One-Pot Synthesis of Indoles through Sequential Hydroamination and Cross-Dehydrogenative Coupling Reaction
Cai, Yichao,Chen, Chunxia,Chen, Xin,Liu, Yajie,Peng, Jinsong,Song, Zirui,Sun, Peng,Yang, Jiaojiao
, p. 75 - 84 (2019/12/26)
Starting from simple anilines and ester arylpropiolates, an efficient one-pot synthesis of 2-arylindole-3-carboxylate derivatives has been developed through copper-mediated sequential hydroamination and cross-dehydrogenative coupling (CDC) reaction. The i
Metal-Free Tandem Rearrangement/Lactonization: Access to 3,3-Disubstituted Benzofuran-2-(3H)-ones
Santi, Micol,Ould, Darren M. C.,Wenz, Jan,Soltani, Yashar,Melen, Rebecca L.,Wirth, Thomas
supporting information, p. 7861 - 7865 (2019/04/25)
A novel metal-free synthesis of 3,3-disubstituted benzofuran-2-(3H)-ones through reacting α-aryl-α-diazoacetates with triarylboranes is presented. Initially, triarylboranes were successfully investigated in α-arylations of α-diazoacetates, however in the presence of a heteroatom in the ortho position, the boron enolate intermediate undergoes an intramolecular rearrangement to form a quaternary center. The intermediate cyclizes to afford valuable 3,3-disubstituted benzofuranones in good yields.