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CAS

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136672-25-8

(1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE, also known as 3-(1H-indol-3-yl)-1-(3-methoxyphenyl)propan-1-one, is a chemical compound that belongs to the category of indole derivatives. It is composed of an indole ring and a 3-methoxyphenyl group attached to a ketone functional group. (1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE has potential biological and pharmacological activities, and it has been studied for its potential therapeutic applications. The structure and properties of (1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE make it a promising candidate for further research in the fields of medicinal chemistry and drug development.

136672-25-8

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136672-25-8 Usage

Uses

Used in Pharmaceutical Industry:
(1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE is used as a pharmaceutical candidate for its potential therapeutic applications due to its biological and pharmacological activities.
Used in Medicinal Chemistry Research:
(1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE is used as a subject of study for its potential applications in medicinal chemistry, given its unique structure and properties.
Used in Drug Development:
(1H-INDOL-3-YL)-(3-METHOXY-PHENYL)-METHANONE is used as a compound of interest in drug development, as its exploration may lead to the creation of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 136672-25-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,6,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136672-25:
(8*1)+(7*3)+(6*6)+(5*6)+(4*7)+(3*2)+(2*2)+(1*5)=138
138 % 10 = 8
So 136672-25-8 is a valid CAS Registry Number.

136672-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indol-3-yl-(3-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 3-(3-Methoxybenzoyl)indole

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:136672-25-8 SDS

136672-25-8Downstream Products

136672-25-8Relevant articles and documents

ARYL HYDROCARBON RECEPTOR MODULATORS AND USES THEREOF

-

Paragraph 00426; 00453, (2019/10/29)

Provided are compounds of Formula (I), and pharmaceutically acceptable salts, solvates, hydrates, stereoisomers, tautomers, isotopically labeled derivatives, polymorphs, and prodrugs thereof, wherein X1-X4, RX, RC, RB, n, and Ring A are as defined herein. The compounds may be aryl hydrocarbon receptor agonists or partial aryl hydrocarbon receptor agonists. Also provided are pharmaceutical compositions comprising a compound of Formula (I) and methods of using such compounds for treating diseases and conditions related to the activity of an aryl hydrocarbon receptor, such as, for example, inflammatory diseases, autoimmune diseases, metabolic disorders, and proliferative diseases.

Mild and selective Ru-catalyzed formylation and Fe-catalyzed acylation of free (N-H) indoles using anilines as the carbonyl source

Wu, Wenliang,Su, Weiping

supporting information; experimental part, p. 11924 - 11927 (2011/09/19)

C3-selective formylation and acylation of free (N-H) indoles under mild conditions can be achieved by using Ru- and Fe-catalyzed oxidative coupling of free (N-H) indoles with anilines, respectively. Both processes are operationally simple, compatible with a variety of functional groups and generally provide the desired products in good yields. 13C-labeling experiments unambiguously established that the carbonylic carbon in the formylation products originated from methyl group of N-methyl aniline.

INDOLE DERIVATIVES AND THEIR USE FOR TESTOSTERONE 5-ALPHA-REDUCTASE-MEDIATED DISEASES

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, (2008/06/13)

Indole derivatives of the formula and pharmaceutical compositions thereof. They are useful for treating or preventing testosterone 5-alpha-reductase-mediated diseases, such as alopecia, acnes and prostatism

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