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850008-37-6

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850008-37-6 Usage

General Description

2-(7-Methoxyindol-1H-3-yl)acetic acid is a chemical compound with the molecular formula C12H11NO3. It is a derivative of indole, a heterocyclic aromatic organic compound. 2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID is a derivative of 7-methoxyindole and acetic acid, with the indole ring containing a methoxy group. It is often used in pharmaceutical research and development due to its potential pharmacological properties. The compound may have potential applications in the treatment of various diseases and disorders, although further research and testing are required to determine its full range of potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 850008-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,0,0 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 850008-37:
(8*8)+(7*5)+(6*0)+(5*0)+(4*0)+(3*8)+(2*3)+(1*7)=136
136 % 10 = 6
So 850008-37-6 is a valid CAS Registry Number.

850008-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-methoxy-1H-indol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (7-methoxy-indol-3-yl)-acetic acid

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:850008-37-6 SDS

850008-37-6Downstream Products

850008-37-6Relevant articles and documents

Three oxidative metabolites of indole-3-acetic acid from Arabidopsis thaliana

Kai, Kenji,Horita, Junko,Wakasa, Kyo,Miyagawa, Hisashi

, p. 1651 - 1663 (2008/02/05)

Three metabolites of indole-3-acetic acid (IAA), N-(6-hydroxyindol-3-ylacetyl)-phenylalanine (6-OH-IAA-Phe), N-(6-hydroxyindol-3-ylacetyl)-valine (6-OH-IAA-Val), and 1-O-(2-oxoindol-3-ylacetyl)-β-d-glucopyranose (OxIAA-Glc), were found by a liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS)-based search for oxidative IAA metabolites during the vegetative growth of Arabidopsis. Their structures were confirmed by making a comparison of chromatographic characteristics and mass spectra between naturally occurring compounds and synthetic standards. An incorporation study using deuterium-labeled compounds showed that 6-OH-IAA-Phe and 6-OH-IAA-Val were biosynthesized from IAA-Phe and IAA-Val, respectively, which strongly suggested the formation of these amino acid conjugates of IAA in plants. Both 6-OH-IAA-Phe and 6-OH-IAA-Val were inactive as auxins, as indicated by no significant root growth inhibition in Arabidopsis. Quantitative analysis demonstrated that OxIAA-Glc was present in the largest amount among the metabolites of IAA in Arabidopsis, suggesting that the conversion into OxIAA-Glc represents the main metabolic process regarding IAA in Arabidopsis.

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