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120191-50-6

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120191-50-6 Usage

Heterocyclic compound

Contains both indole and oxazole rings

Biological activities

Exhibits antimicrobial, antifungal, and anticancer activities

Pharmacological properties

Has potential for drug discovery and development

Medicinal chemistry

Investigated for potential use in medicinal chemistry

Building block

Used in the synthesis of various organic compounds

Importance

A significant chemical compound in medicinal and pharmaceutical research due to its diverse biological and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 120191-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,9 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 120191-50:
(8*1)+(7*2)+(6*0)+(5*1)+(4*9)+(3*1)+(2*5)+(1*0)=76
76 % 10 = 6
So 120191-50-6 is a valid CAS Registry Number.

120191-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1H-indol-3-yl)-1,3-oxazole

1.2 Other means of identification

Product number -
Other names -

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:120191-50-6 SDS

120191-50-6Relevant articles and documents

Reaction of 3/2-formylindoles with TOSMIC: Formation of indolyloxazoles and stable indolyl primary enamines

Chakrabarty, Manas,Basak, Ramkrishna,Harigaya, Yoshihiro,Takayanagi, Hiroaki

, p. 1793 - 1801 (2005)

3-Formylindole and its 1-substituted and 1,5-disubstituted derivatives react with TOSMIC in presence of potassium carbonate in methanol under reflux to furnish 5-(3′-indolyl)oxazoles, new stable E-2-(3′-indolyl)-2- tosylethenamines and two diastereomers of N-[2-(3′-indolyl)-1,2-dimethoxy] ethylformamides. In contrast, 2-formylskatole furnishes N-(1-tosyl-2-skatolyl) ethenylformamide.

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