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109175-08-8

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109175-08-8 Usage

Description

1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is a versatile chemical compound belonging to the indole class of organic compounds. It is a methyl ester derivative of 4-nitro-1H-indole-3-carboxylic acid, characterized by its nitro group, which makes it a valuable molecule for medicinal chemistry. 1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is widely recognized for its potential in the synthesis of pharmaceuticals and agrochemicals, serving as a starting material for various biologically active compounds. Its diverse applications and importance in the field of organic chemistry make it a significant compound for research and development.

Uses

Used in Pharmaceutical Industry:
1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is used as a starting material for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups enable the development of new drugs with potential therapeutic applications. The nitro group in this compound allows for further chemical modifications, facilitating the creation of diverse drug candidates with improved pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is utilized as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to form biologically active compounds makes it a valuable component in the development of effective and environmentally friendly agrochemical products.
Used in Medicinal Chemistry Research:
1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is employed as a key intermediate in medicinal chemistry research. Its versatility and potential for diverse applications make it an important compound for exploring new chemical entities and understanding their biological activities. Researchers use this compound to investigate its interactions with various biological targets, leading to the discovery of novel therapeutic agents.
Used in Organic Chemistry Education:
As a representative of the indole class of organic compounds, 1H-Indole-3-carboxylic acid, 4-nitro-, methyl ester is used in organic chemistry education to teach students about the synthesis, reactions, and properties of indole derivatives. Its functional groups and reactivity provide valuable insights into the principles of organic chemistry and help students develop a deeper understanding of the subject.

Check Digit Verification of cas no

The CAS Registry Mumber 109175-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,1,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109175-08:
(8*1)+(7*0)+(6*9)+(5*1)+(4*7)+(3*5)+(2*0)+(1*8)=118
118 % 10 = 8
So 109175-08-8 is a valid CAS Registry Number.

109175-08-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-nitro-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 4-nitroindole-3-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109175-08-8 SDS

109175-08-8Upstream product

109175-08-8Relevant articles and documents

SYNTHETIC STUDIES ON TELEOCIDIN I. REGIOSELECTIVE INTRODUCTION OF 4-AMINO AND 7-ACYL GROUPS ON INDOLE DERIVATIVE

Nakatsuka, Shin-ichi,Masuda, Toshiya,Asano, Osamu,Teramae, Tomohiro,Goto, Toshio

, p. 4327 - 4330 (1986)

Nitration of indole-3-carboxylic esters, 3 and 9, afforded 4-nitro derivatives, 4 and 10. 10 was regioselectively derived to 15, which contains substituents at 4- and 7-positions of indole nucleus similary to teleocidins.

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