Agrochemicals

Methyl 1H-indole-2-carboxylate

  • CAS:1202-04-6
  • purity:99%
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1.What is the Methyl 1H-indole-2-carboxylate ?

Methyl 1H-indole-2-carboxylate is a chemical compound with the molecular formula C10H9NO2. It belongs to the class of organic compounds known as indole carboxylic acids and derivatives, which are organic compounds containing an indole moiety carrying a carboxylic acid group. Methyl 1H-indole-2-carboxylate is recognized for its potential in exhibiting a wide range of biological activities and is a subject of ongoing research in the pharmaceutical industry.

2.What is the CAS number for Methyl 1H-indole-2-carboxylate ?

The CAS number of Methyl 1H-indole-2-carboxylate is 1202-04-6.

3.What are another words for Methyl 1H-indole-2-carboxylate ?

Synonyms?for?Methyl 1H-indole-2-carboxylate 1202-04-6:Indole-2-carboxylicacid, methyl ester (6CI,7CI,8CI);2-(Methoxycarbonyl)indole;Methyl 2-indolecarboxylate;NSC 78006;

4.What is Methyl 1H-indole-2-carboxylate (1202-04-6) used for?

Used in Pharmaceutical Industry:
Methyl 1H-indole-2-carboxylate is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, Methyl 1H-indole-2-carboxylate serves as a key intermediate in the synthesis of various agrochemicals, playing a crucial role in the creation of effective and innovative products for agricultural applications.
Used in Fragrance Industry:
Methyl 1H-indole-2-carboxylate is also utilized as a fragrance ingredient in perfumes and other cosmetic products. Its distinct scent profile adds depth and complexity to fragrance formulations, enhancing the sensory experience of consumers.
Used in Cosmetic Products:
In the cosmetic industry, Methyl 1H-indole-2-carboxylate is employed for its potential to contribute to the overall effectiveness and appeal of products. Its inclusion in formulations can provide both functional and aesthetic benefits, making it a versatile component in the development of skincare and beauty products.
The diverse applications of Methyl 1H-indole-2-carboxylate highlight its versatility and importance across various industries, from pharmaceuticals and agrochemicals to fragrances and cosmetics. Its ongoing research and development underscore its potential to contribute to future innovations in these fields.

InChI:InChI=1/C10H9NO2/c1-13-10(12)9-6-7-4-2-3-5-8(7)11-9/h2-6,11H,1H3

Relevant articles related to Methyl 1H-indole-2-carboxylate:

Article

Source

Metal-free N-arylation of indolines with diaryliodonium salts

Riedmüller, Stefan,Nachtsheim, Boris J.

, p. 651 - 655 (2015)

Synthesis, spectroscopic identification and molecular docking of certain N-(2-[2-(1H-Indol-2-ylcarbonyl) hydrazinyl](oxo)acetyl phenyl)acetamides and N-[2-(2-[2-(Acetylamino)phenyl](oxo)acetyl hydrazinyl)-2-oxoethyl]-1H-indole-2-carboxamides: New antimicrobial agents

Almutairi, Maha S.,Zakaria, Azza S.,Al-Wabli, Reem I.,Hubert Joe,Abdelhameed, Ali S.,Attia, Mohamed I.

, (2018)

1H-Azirines as Intermediates in the Photolysis of 1,2,3-Triazoles

Mitchell, Glynn,Rees, Charles W.

, p. 399 - 401 (1986)

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