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73177-32-9

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73177-32-9 Usage

Compound Class

Indole class of organic compounds.

Molecular Structure

Bicyclic structure with a six-membered benzene ring fused to a five-membered pyrrole ring.

Versatile Reactivity

Commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and organic materials.

Potential Applications

Material science and dye intermediate.

Biological Activities

Studied for potential anti-inflammatory, anti-cancer, and anti-microbial properties.

Research Interest

Compound of interest for medicinal and biological research.

Check Digit Verification of cas no

The CAS Registry Mumber 73177-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,7 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73177-32:
(7*7)+(6*3)+(5*1)+(4*7)+(3*7)+(2*3)+(1*2)=129
129 % 10 = 9
So 73177-32-9 is a valid CAS Registry Number.

73177-32-9SDS

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 2-Methyl-6-phenylindole

1.2 Other means of identification

Product number -
Other names 1H-INDOLE, 2-METHYL-6-PHENYL-

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:73177-32-9 SDS

73177-32-9Downstream Products

73177-32-9Relevant articles and documents

Preparation method of indole compound

-

Paragraph 0058-0059, (2020/12/29)

The invention discloses a preparation method of a novel efficient indole compound, which comprises the following steps: by using o-nitroalkylbenzene containing various substituents as a raw material,controlling the reaction temperature to be 70-160 DEG C in an organic solution under the protection of inert gas and the participation of inorganic base, thereby obtaining the indole compound; preparing the novel indole compound containing various substituent groups through a hydrocarbon activation reaction catalyzed by a metal rhodium catalyst. The synthetic method is not reported in literature,the raw materials are easy to synthesize, no reducing agent needs to be added additionally, the method is simple in step, the indole compound containing various substituent groups does not need to beconstructed in one step through a nitroso intermediate, and the yield is high; The method is simple in unit operation, low in equipment requirement and suitable for rapidly synthesizing the indole compounds containing various substituent groups.

Indole Synthesis via SRN1 Reactions

Bard, Raymond R.,Bunnett, Joseph F.

, p. 1546 - 1547 (2007/10/02)

o-Haloanilines react with ketone enolate ions in ammonia under irradiation to form indoles in good yields.

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