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1025760-25-1

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1025760-25-1 Usage

Derivative of indole

Heterocyclic aromatic compound The molecule is derived from the indole structure, which is a common compound found in plants and features a heterocyclic aromatic ring.

Usage in synthesis

Pharmaceutical, agrochemical, and dye industries This chemical is often utilized in the production of various products, such as pharmaceuticals, agrochemicals, and dyes, due to its unique structure and properties.

Biological activities

Anti-inflammatory and antioxidant properties The compound has been found to exhibit potential biological activities, including reducing inflammation and neutralizing harmful free radicals.

Building block in organic synthesis

Creating complex molecules 1-Methyl-1H-indole-3-carboxylic acid butyl ester can be used as a starting material to build more complex organic molecules with diverse applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1025760-25-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,7,6 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1025760-25:
(9*1)+(8*0)+(7*2)+(6*5)+(5*7)+(4*6)+(3*0)+(2*2)+(1*5)=121
121 % 10 = 1
So 1025760-25-1 is a valid CAS Registry Number.

1025760-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl 1-methyl-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-methyl-1H-indole-3-carboxylic acid butyl ester

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:1025760-25-1 SDS

1025760-25-1Downstream Products

1025760-25-1Relevant articles and documents

Palladium-catalyzed oxidative cyclization of tertiary enamines for synthesis of 1,3,4-trisubstituted pyrroles and 1,3-disubstituted indoles

Lian, Xiao-Li,Ren, Zhi-Hui,Wang, Yao-Yu,Guan, Zheng-Hui

supporting information, p. 3360 - 3363 (2014/07/08)

A novel and efficient palladium-catalyzed intramolecular oxidative cyclization of tertiary enamines for the synthesis of 1,3,4-trisubstituted pyrroles and 1,3-disubstituted indoles has been developed. Trifluoroacetic acid plays an important role in the reaction. A series of pyrroles and indoles with substitution patterns that are not easily accessible by traditional routes were synthesized in good yields under mild conditions.

Regioselective Rh-catalyzed direct carbonylation of indoles to synthesize indole-3-carboxylates

Lang, Rui,Wu, Junliang,Shi, Lijun,Xia, Chungu,Li, Fuwei

supporting information; experimental part, p. 12553 - 12555 (2012/02/02)

Rh-catalyzed C-H carbonylation of indoles under 1 atm of CO has been achieved. Various substituted indoles and indole with free N-H could be carboxylated with linear- and/or cyclic-alcohol to give the desired indole-3-carboxylates with up to 92% yield. A mechanism involving Rh III initiated C-H metallation is proposed.

Copper-catalyzed synthesis of esters from ketones. Alkyl group as a leaving group

Nakatani, Yuji,Koizumi, Yuichiro,Yamasaki, Ryu,Saito, Shinichi

supporting information; experimental part, p. 2067 - 2070 (2009/04/08)

The conversion of ketones to esters has been achieved through the use of Cu catalyst and tetrabutylammonium nitrite. This reaction involves the activation of the less activated C-C bond, and the alkyl group is removed as a leaving group. Various isopropyl ketones are found to be good substrates for this reaction.

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