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7-Methoxy-1H-indole-2-carboxylic acid is an indole derivative with the molecular formula C10H9NO3, featuring a carboxylic acid group and a methoxy group attached to the aromatic ring. It serves as a crucial building block in the synthesis of pharmaceutical compounds and organic molecules, playing a significant role in the development of new drugs and pharmaceutical products within the pharmaceutical industry.

24610-33-1

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24610-33-1 Usage

Uses

Used in Pharmaceutical Industry:
7-Methoxy-1H-indole-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential biological activities and pharmacological properties. It contributes to the development of new drugs and pharmaceutical products, enhancing their therapeutic efficacy and applications.
Used in Medicinal Chemistry Research and Development:
7-METHOXY-1H-INDOLE-2-CARBOXYLIC ACID is utilized as an important substance in research and development within the field of medicinal chemistry. Its unique structure and properties make it a valuable tool for exploring novel drug candidates and understanding their mechanisms of action, thereby advancing the discovery of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 24610-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24610-33:
(7*2)+(6*4)+(5*6)+(4*1)+(3*0)+(2*3)+(1*3)=81
81 % 10 = 1
So 24610-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c1-14-8-4-2-3-6-5-7(10(12)13)11-9(6)8/h2-5,11H,1H3,(H,12,13)

24610-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-METHOXY-1H-INDOLE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 7-Methoxy-indol-2-carbonsaeure

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:24610-33-1 SDS

24610-33-1Relevant academic research and scientific papers

INDOLE DERIVATIVES AND DRUGS CONTAINING THE SAME

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Page/Page column 9, (2010/02/11)

An indole derivative represented by the following general formula (1) : wherein at least one of R1, R2, R3, and R4 represents an alkoxy group containing 1 to 20 carbon atoms, and other groups of the R1, R2, R3, and R4 represent hydrogen, an alkyl group containing 1 to 6 carbon atoms, acetyl group, or hydroxyl group; and either one of X and Y represents -(CH2)nOH wherein n is an integer of 0 to 30, and the other one of the X and Y represents hydrogen atom; or a salt thereof; and a drug and an agent for promoting differentiation of a stem cell containing such indole derivative or its salt as an effective component. The indole derivative (1) of the present invention has action of inducing differentiation of neural stem cell specifically into a neuron, and this indole derivative is useful as a prophylactic or therapeutic drug for brain dysfunction or neuropathy caused by loss or degeneration of the neuron.

USE OF INDOLYL DERIVATIVES FOR THE MANUFACTURE OF A MEDICAMENT FOR THE TREATMENT ALLERGIC RHINITIS

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Page/Page column 75-77, (2008/06/13)

A method to treat allergic rhinitis is disclosed in which patients are administered certain indolyl compounds.

Effects of indole fatty alcohols on the differentiation of neural stem cell derived neurospheres

Coowar, Djalil,Bouissac, Julien,Hanbali, Mazen,Paschaki, Marie,Mohier, Eliane,Luu, Bang

, p. 6270 - 6282 (2007/10/03)

In a search for inducers of neuronal differentiation to treat neurodegenerative diseases such as Alzheimer's disease, a series of indole fatty alcohols (IFAs) were prepared, 13c (n = 18) was able to promote the differentiation of neural stem cell derived neurospheres into neurons at a concentration of 10 nM. Analysis of the expression of the Notch pathway genes in neurospheres treated during the differentiation phase with 13c (n = 18) revealed a significant decrease in the transcription of the Notch 4 receptor.

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