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7510-15-8

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7510-15-8 Usage

Description

(5-methoxy-1-methyl-1H-indol-3-yl)acetic acid is a chemical compound that features an indole ring and a carboxylic acid group. It is a derivative of serotonin, a neurotransmitter that is integral in the regulation of mood, appetite, and sleep.

Uses

Used in Pharmaceutical Industry:
(5-methoxy-1-methyl-1H-indol-3-yl)acetic acid is used as a potential therapeutic agent for the treatment of mood disorders and depression. Its role as a serotonin derivative suggests it may help in modulating neurotransmission and alleviating symptoms associated with these conditions.
Used in Gastroenterology:
In the field of gastroenterology, (5-methoxy-1-methyl-1H-indol-3-yl)acetic acid is studied for its potential role in regulating gastrointestinal function. Its effects on gastrointestinal motility and secretion could be beneficial for treating various gastrointestinal disorders.
Used in Inflammation Management:
(5-methoxy-1-methyl-1H-indol-3-yl)acetic acid is also being investigated for its potential in managing inflammation. Given its structural relation to serotonin, it may have implications for conditions where inflammatory processes are involved, offering a new avenue for therapeutic intervention.
These applications highlight the compound's versatility and the need for further research to fully understand and harness its potential in medical and pharmaceutical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 7510-15-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7510-15:
(6*7)+(5*5)+(4*1)+(3*0)+(2*1)+(1*5)=78
78 % 10 = 8
So 7510-15-8 is a valid CAS Registry Number.

7510-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-methoxy-1-methylindol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names <1-Methyl-5-methoxy-indolyl-(3)>-essigsaeure

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:7510-15-8 SDS

7510-15-8Relevant articles and documents

Substituted Heteroaromatic Carboxamide and Urea Compounds as Vanilloid Receptor Ligands

-

, (2012/05/20)

Substituted heteroaromatic carboxamide and urea compounds corresponding to formula (i) processes for the preparation thereof, pharmaceutical compositions containing these compounds and also a method of using these compounds in pharmaceutical compositions for treating or inhibiting pain and other conditions mediated at least in part via the vanilloid receptor 1.

Organocatalyzed enantioselective fluorocyclizations

Lozano, Oscar,Blessley, George,Martinez Del Campo, Teresa,Thompson, Amber L.,Giuffredi, Guy T.,Bettati, Michela,Walker, Matthew,Borman, Richard,Gouverneur, Veronique

supporting information; experimental part, p. 8105 - 8109 (2011/10/03)

Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral indoles (see scheme; Ts=tosyl, Bn=benzyl, Boc=tert-butoxycarbonyl). More than twenty examples for this cascade fluorination-cyclization, which is catalyzed by cinchona alkaloids and employs N-fluorobenzenesulfonimide as the electrophilic fluorine source have been explored, and an unprecedented catalytic asymmetric difluorocyclization has also been identified.

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