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61989-29-5

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61989-29-5 Usage

General Description

1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-, methyl ester, is a chemical compound with the formula C11H11NO3. It is a derivative of the plant hormone indole-3-acetic acid (IAA), which plays a crucial role in the regulation of plant growth and development. The methyl ester form of 1H-Indole-3-acetic acid can be used to study the biological activities and physiological effects of IAA in plants. It is commonly used in research and experimental settings to investigate the role of IAA in plant biology and to understand the mechanisms underlying plant growth and development. 1H-Indole-3-acetic acid, 2,3-dihydro-2-oxo-, methyl ester has potential applications in agriculture and horticulture for the regulation of plant growth and the enhancement of crop yield.

Check Digit Verification of cas no

The CAS Registry Mumber 61989-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,8 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61989-29:
(7*6)+(6*1)+(5*9)+(4*8)+(3*9)+(2*2)+(1*9)=165
165 % 10 = 5
So 61989-29-5 is a valid CAS Registry Number.

61989-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(2-oxo-1,3-dihydroindol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names oxindole-3-acetic acid methyl 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:61989-29-5 SDS

61989-29-5Relevant articles and documents

Convergent synthesis of dihydroquinolones from o-aminoarylboronates

Horn, Joachim,Li, Ho Yin,Marsden, Stephen P.,Nelson, Adam,Shearer, Rachel J.,Campbell, Amanda J.,House, David,Weingarten, Gordon G.

experimental part, p. 9002 - 9007 (2009/12/22)

An efficient and convergent one-step synthesis of substituted dihydroquinolin-2-ones from α,β-unsaturated esters and aminoaryl pinacolboronates under rhodium catalysis is reported. The reaction is easily applicable in parallel synthesis format and provide

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