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131057-63-1

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131057-63-1 Usage

General Description

2H-Indol-2-one, 5-ethoxy-1,3-dihydro-1,3-dimethyl-(9CI) is a chemical compound with the molecular formula C13H15NO2. It is a derivative of 2H-indol-2-one with an ethoxy group at the 5th position and two methyl groups at the 1st and 3rd positions of the dihydroindolone ring. 2H-Indol-2-one,5-ethoxy-1,3-dihydro-1,3-dimethyl-(9CI) may have potential pharmaceutical applications, as it exhibits pharmacological activities and may be used as a building block in organic synthesis. Its specific properties and uses depend on its structure and chemical reactivity, making it a subject of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 131057-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,5 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 131057-63:
(8*1)+(7*3)+(6*1)+(5*0)+(4*5)+(3*7)+(2*6)+(1*3)=91
91 % 10 = 1
So 131057-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO2/c1-4-15-9-5-6-11-10(7-9)8(2)12(14)13(11)3/h5-8H,4H2,1-3H3

131057-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-5-ethoxyoxindole

1.2 Other means of identification

Product number -
Other names 5-ETHOXY-1,3-DIMETHYL-1,3-DIHYDRO-INDOL-2-ONE

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:131057-63-1 SDS

131057-63-1Downstream Products

131057-63-1Relevant articles and documents

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Julian,Pikl

, p. 563,566 (1935)

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Process for the enantioselective synthesis of intermediates used in the preparation of physostigmine

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, (2008/06/13)

This invention relates to a process of obtaining optically pure enantiomers of an alkylated oxindole selected from STR1 where R is methyl, ethyl or benzyl.

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