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1-Methyl-3-nitro-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36728-89-9

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36728-89-9 Usage

Synthesis Reference(s)

Synthesis, p. 1117, 1999 DOI: 10.1055/s-1999-3512

Check Digit Verification of cas no

The CAS Registry Mumber 36728-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,2 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 36728-89:
(7*3)+(6*6)+(5*7)+(4*2)+(3*8)+(2*8)+(1*9)=149
149 % 10 = 9
So 36728-89-9 is a valid CAS Registry Number.

36728-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-nitroindole

1.2 Other means of identification

Product number -
Other names 1-Methyl-3-nitro-1H-indole

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:36728-89-9 SDS

36728-89-9Relevant academic research and scientific papers

ISOQUINOLINE DERIVATIVES AS PROTEIN KINASE INHIBITORS

-

, (2021/02/12)

The present invention relates to a compound suitable for use as a kinase inhibitor

Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives

Laugeois, Maxime,Ling, Johanne,Férard, Charlène,Michelet, Véronique,Ratovelomanana-Vidal, Virginie,Vitale, Maxime R.

supporting information, p. 2266 - 2269 (2017/05/12)

The palladium(0)-catalyzed diastereoselective dearomative cyclopentannulation of 3-nitroindoles with vinylcyclopropanes is described. This straightforward and highly atom-economical method leads to a wide range of functionalized indolines in good yields a

Convenient synthesis of masked aminoindoles by indium mediated one-pot reductive acylation of 3- and 2-nitroindoles

Roy, Sujata,Gribble, Gordon W.

, p. 51 - 56 (2007/10/03)

Unstable 3- and 2-aminoindoles arc generated in situ by indium mediated reduction of 3- and 2-nitroindoles and capped as the stable amides (or carbamate) in moderate to high yields under mild conditions in a one-pot procedure.

Synthesis and reactions of N-protected 3-nitroindoles

Pelkey,Gribble

, p. 1117 - 1122 (2007/10/03)

Treatment of N-protected indoles 3 with acetyl nitrate generated in situ at low temperatures affords the corresponding 3-nitroindoles 2 in good to excellent yields. Deprotection of 1-acetyl-3-nitroindole (2h) with DBU gives 3-nitroindole (1). Reaction of

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