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Ethyl (5-nitro-1H-indol-3-yl)acetate is an organic compound with the chemical formula C12H12N2O4. It is a derivative of indole, a heterocyclic aromatic organic compound, and features a nitro group at the 5-position and an acetate group at the 3-position. This yellow crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of indole-based compounds with potential biological activities. The compound is characterized by its melting point of 95-97°C and is soluble in common organic solvents such as ethanol, methanol, and acetone. Due to its reactivity and potential applications, ethyl (5-nitro-1H-indol-3-yl)acetate is an important building block in the field of organic chemistry and drug development.

6970-51-0

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6970-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6970-51-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6970-51:
(6*6)+(5*9)+(4*7)+(3*0)+(2*5)+(1*1)=120
120 % 10 = 0
So 6970-51-0 is a valid CAS Registry Number.

6970-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name <5-Nitro-indolyl-(3)>-essigsaeureethylester

1.2 Other means of identification

Product number -
Other names CARBAZIC ACID,3-(5-NITROFURFURYLIDENE)-,2-HYDROXYETHYL 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:6970-51-0 SDS

6970-51-0Relevant academic research and scientific papers

Fe-catalyzed Fukuyama-type indole synthesis triggered by hydrogen atom transfer

Huang, Hanmin,Yu, Min,Zhang, Tianze

, p. 10501 - 10505 (2021/08/20)

Fe, Co, and Mn hydride-initiated radical olefin additions have enjoyed great success in modern synthesis, yet the extension of other hydrogen radicalophiles instead of olefins remains largely elusive. Herein, we report an efficient Fe-catalyzed intramolec

Indole-3-acetic acids and hetero analogues by one pot synthesis including Heck cyclisation

Wensbo, David,Annby, Ulf,Gronowitz, Salo

, p. 10323 - 10342 (2007/10/02)

Bz-substituted indole-3-acetic acid ethyl esters (14e-g) and heteroanalogues, i.e. thienopyrroles (14a,c) and selenolopyrrole (14d), were prepared starting from N-BOC protected o-iodo aryl amines. Allylation with ethyl 4-bromocrotonate, followed by palladium-catalysed ring closure in a one pot reaction, yielded N-BOC protected indoles (13e-g), thienopyrroles (13a-c), and selenolopyrrole (13d). The BOC group was readily removed thermally after adsorption on silica. Oxothienopyrroles (11a-c) were similarly prepared.

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