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[1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI) is a heterocyclic chemical compound with the molecular formula C8H6N2O. It is characterized by its nitrogen and oxygen atoms in its ring structure, which contribute to its unique properties and potential applications in various fields.

67506-48-3

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67506-48-3 Usage

Uses

Used in Organic Synthesis:
[1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse properties and applications.
Used in Materials Science:
In the field of materials science, [1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI) is used as a component in the development of new materials with specific properties. Its incorporation into these materials can lead to enhanced performance in areas such as electronics, optics, and energy storage.
Used in Anticancer Applications:
[1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI) has been investigated for its potential as an anticancer agent. Its unique structure and properties make it a promising candidate for further research and development in the fight against cancer.
Used in Pharmaceutical Research:
[1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI)'s pharmacological activities have been studied, and [1,2,5]Oxadiazolo[3,4-b]quinoxaline (9CI) is used as a starting point for the development of new drugs. Its potential applications in the pharmaceutical industry could lead to the creation of novel therapeutics for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 67506-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67506-48:
(7*6)+(6*7)+(5*5)+(4*0)+(3*6)+(2*4)+(1*8)=143
143 % 10 = 3
So 67506-48-3 is a valid CAS Registry Number.

67506-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name furazano[3,4-b]quinoxaline

1.2 Other means of identification

Product number -
Other names furazono[3,4-b]quinoxaline

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:67506-48-3 SDS

67506-48-3Relevant academic research and scientific papers

REACTIONS OF FUROXANS WITH PHOSPHORUS YLIDES

Argyropoulos, N. G.,Gallos, J. K.,Nicolaides, D. N.

, p. 3631 - 3636 (2007/10/02)

Benzofuroxan (1) reacts with phosphorus ylide 2 to give benzimidazole derivatives 8 and 10, whereas reaction of 1 with ylide 12 furnishes quinoxaline 17 via an initial Wittig-type reaction.Similarly the reaction between the furoxanoquinoxalines 19a or 19b and the ylide 2 yielded compounds 22a and 22b, respectively.In these reactions as well as in the reactions of the above furoxans with other phosphorus ylides, a significant deoxygenation of the furoxans to furazans with subsequent oxidation of the ylides is generally observed.

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