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8H-Isoxazolo[5,4-b]indole, also known as 8H-isoxazolo[5,4-b]indole(8CI,9CI), is a chemical compound with the molecular formula C9H6N2O. It belongs to the class of organic compounds known as isoxazoloindoles, which are fused heterocyclic compounds consisting of an isoxazole ring attached to an indole ring. This specific compound is characterized by its unique structure, where the isoxazole ring is fused to the indole at the 5,4-b position. 8H-Isoxazolo[5,4-b]indole is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its diverse chemical properties and potential applications in drug design.

247-06-3

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247-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 247-06-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 247-06:
(5*2)+(4*4)+(3*7)+(2*0)+(1*6)=53
53 % 10 = 3
So 247-06-3 is a valid CAS Registry Number.

247-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 8H-isoxazolo[5,4-b]indole

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

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More Details:247-06-3 SDS

247-06-3Downstream Products

247-06-3Relevant academic research and scientific papers

Microwave-assisted one-pot synthesis of pyrazolo[3,4- b]indoles and new isoxazolo[5,4- b]indoles via copper-catalyzed intramolecular C-N/C-O bond formation

Kumar, Arepalli Sateesh,Rao, P. V. Amulya,Nagarajan, Rajagopal

experimental part, p. 3878 - 3886 (2012/01/05)

A facile one-pot, two-step synthesis of highly substituted pyrazolo[3,4-b]indoles and isoxazolo[5,4-b]indoles was developed via microwave-assisted, copper-catalyzed intramolecular heterocyclization (involving C-N/C-O bond formation) from 3-acetyl-2-chloroindoles in good to excellent yields. Georg Thieme Verlag Stuttgart. New York.

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