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61394-49-8

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61394-49-8 Usage

General Description

Ethyl 2-oxoindoline-5-carboxylate is a chemical compound with the molecular formula C11H11NO3. It is a derivative of indole, a heterocyclic compound commonly found in plants and natural products. Ethyl 2-oxoindoline-5-carboxylate is used as a building block in organic synthesis and pharmaceutical research, particularly in the development of drugs targeting dopamine receptors in the central nervous system. Ethyl 2-oxoindoline-5-carboxylate has also been investigated for its potential anti-inflammatory and anticancer properties. Its structure and reactivity make it a versatile starting material for the synthesis of various biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 61394-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,9 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61394-49:
(7*6)+(6*1)+(5*3)+(4*9)+(3*4)+(2*4)+(1*9)=128
128 % 10 = 8
So 61394-49-8 is a valid CAS Registry Number.

61394-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-1,3-dihydroindole-5-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 2-oxoindoline-5-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:61394-49-8 SDS

61394-49-8Relevant articles and documents

An efficient synthesis of a spirocyclic oxindole analogue

Teng, Dawei,Zhang, Hongxing,Mendonca

, p. 700 - 706 (2006)

An efficient, scaleable synthesis approach towards the spirocyclic oxindole analogue 1′-(tert-butoxycarbonyl)-2-oxospiro[indoline-3,4′- piperidine]-5-carboxylic acid (1) is described. The key steps are dianion alkylation and cyclization of ethyl 2-oxindoline-5-carboxylate (4) and demethylation of the resulting spirocyclic oxindole ethyl 1′-methyl-2- oxospiro[indoline-3,4′-piperidine]-5-carboxylate (5). The target compound was obtained in an overall yield of 35 % over eight steps without resorting to chromatographic purification.

Studies on positive inotropic agents. V. Synthesis of 1-heteroaroylpiperazine derivatives

Ogawa,Tamada,Fujioka,Teramoto,Kondo,Yamashita,Yabuuchi,Tominaga,Nakagawa

, p. 2253 - 2258 (2007/10/02)

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