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1H-Indole-2-carboxaldehyde, 3-chloro-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126309-77-1

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126309-77-1 Usage

Derivative of indole

A heterocyclic aromatic compound

Contains a 3-chloro-1-methyl group

A chlorine atom attached to the third carbon and a methyl group attached to the first carbon

Commonly used in synthesis

Used in the production of pharmaceuticals, agrochemicals, and other organic compounds

Potential antibacterial and antifungal properties

Has been studied for its ability to inhibit the growth of bacteria and fungi

Derivatives have shown potential for treating various diseases and medical conditions

Variants of 1H-Indole-2-carboxaldehyde, 3-chloro-1-methyl- have demonstrated potential for therapeutic use

Used in development of fluorescent probes and dyes for biological imaging and diagnostics

Utilized in creating compounds that can be used to visualize and diagnose biological processes and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 126309-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126309-77:
(8*1)+(7*2)+(6*6)+(5*3)+(4*0)+(3*9)+(2*7)+(1*7)=121
121 % 10 = 1
So 126309-77-1 is a valid CAS Registry Number.

126309-77-1SDS

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 3-chloro-1-methylindole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-chloro-N-methylindole-2-carboxaldehyde

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:126309-77-1 SDS

126309-77-1Relevant academic research and scientific papers

Chemistry of polyhalogenated nitrobutadienes, part 11: Ipso-formylation of 2-chlorothiophenes under Vilsmeier-Haack conditions

Vogt, Eva-Janina,Zapol'skii, Viktor A.,Nutz, Eva,Kaufmann, Dieter E.

experimental part, p. 285 - 294 (2012/07/14)

The regioselective ipso-formylation of electron-rich, 3,4-push-pull- substituted 2-chlorothiophenes under Vilsmeier-Haack conditions was performed in good yields. The synthetic scope of this new reaction was explored using various halothiophenes, chloroanilines, and 1-methyl-3-chloroindole. In comparison with their structural C-H analogs the chlorinated thiophenes, anilines, and the indole proved to be less reactive toward electrophilic attack by chloromethyleniminium salts.

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