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194231-75-9

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194231-75-9 Usage

Derivative of indole

A heterocyclic compound commonly found in nature and known for its diverse pharmacological activities.

Unique properties

Presence of 7-bromo and 3,4-dimethoxybenzoyl groups.

Potential applications

Pharmaceutical, agrochemical, and materials science fields.

Biological activities

Antibacterial, antifungal, and anti-inflammatory properties.

Use as building block

In the synthesis of biologically active molecules.

Interesting target

For further research and study due to its structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 194231-75-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 194231-75:
(8*1)+(7*9)+(6*4)+(5*2)+(4*3)+(3*1)+(2*7)+(1*5)=139
139 % 10 = 9
So 194231-75-9 is a valid CAS Registry Number.

194231-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (7-bromoindol-1-yl)-(3,4-dimethoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 1H-Indole,7-bromo-1-(3,4-dimethoxybenzoyl)

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:194231-75-9 SDS

194231-75-9Relevant articles and documents

A new approach to pyrrolophenanthridone alkaloids via intramolecular radical cyclization

Tsuge, Otohiko,Hatta, Taizo,Tsuchiyama, Hiroshi

, p. 155 - 156 (2007/10/03)

A new approach to the synthesis of pyrrolophenanthridone class of alkaloids is described. The method is based on intramolecular radical cyclization of easily accessible 1-aroyl-7-bromoindoles with Bu3SnH and AIBN.

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