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5526-13-6

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5526-13-6 Usage

General Description

7-Acetoxyindole is a chemical compound with the molecular formula C10H9NO2. It is a derivative of indole, a heterocyclic organic compound. 7-Acetoxyindole is primarily used in research and pharmaceutical applications. It has been studied for its potential therapeutic properties, including its anti-inflammatory and antioxidant effects. The compound has also been investigated for its potential as a precursor in the synthesis of biologically active molecules. 7-Acetoxyindole is of interest to scientists and researchers seeking to develop new drugs and therapeutic interventions.

Check Digit Verification of cas no

The CAS Registry Mumber 5526-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,2 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5526-13:
(6*5)+(5*5)+(4*2)+(3*6)+(2*1)+(1*3)=86
86 % 10 = 6
So 5526-13-6 is a valid CAS Registry Number.

5526-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indol-7-yl acetate

1.2 Other means of identification

Product number -
Other names 7-Acetoxy-indol

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:5526-13-6 SDS

5526-13-6Downstream Products

5526-13-6Relevant articles and documents

Synthesis of Indole-Dihydroisoquinoline Sulfonyl Ureas via Three-Component Reactions

Pearson, Stuart E.,Fillery, Shaun M.,Goldberg, Kristin,Demeritt, Julie E.,Eden, Jonathan,Finlayson, Jonathan,Patel, Anil

, p. 4963 - 4981 (2018/12/13)

Isoquinolines activated with sulfamoyl chlorides were reacted with indoles in a 3-component reaction to generate a library of dihydroisoquinoline derivatives. Using a differential protecting group strategy, products could be further derivatised. Synthesis of isoquinoline starting materials using several different methods is also described.

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