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3-AminoIsoxazolo[4,5-b]Pyrazine is a chemical compound characterized by the presence of pyrazine and isoxazole functional groups. Pyrazines are known for their aromatic properties and are responsible for the flavors and aromas in various foods like chocolate, coffee, and fruits. Isoxazoles are organic compounds with diverse biological activities, suggesting potential therapeutic applications. However, detailed information on the physical and chemical properties or specific uses of 3-AminoIsoxazolo[4,5-b]Pyrazine is not extensively documented in the literature.

81411-79-2

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81411-79-2 Usage

Uses

Given the limited information available, the potential uses of 3-AminoIsoxazolo[4,5-b]Pyrazine can be inferred based on the properties of its constituent functional groups:
Used in Flavor and Fragrance Industry:
3-AminoIsoxazolo[4,5-b]Pyrazine is used as a flavoring agent for its aromatic properties, contributing to the rich taste and smell in food products, particularly those with chocolate, coffee, or fruity notes.
Used in Pharmaceutical Industry:
3-AminoIsoxazolo[4,5-b]Pyrazine is used as a potential therapeutic compound due to the biological activities associated with isoxazoles, which may offer opportunities for the development of new drugs or treatments.
Used in Chemical Research:
3-AminoIsoxazolo[4,5-b]Pyrazine serves as a subject of study in chemical research, where its properties and potential applications are explored to expand the understanding of its role in various chemical and biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 81411-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,1 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81411-79:
(7*8)+(6*1)+(5*4)+(4*1)+(3*1)+(2*7)+(1*9)=112
112 % 10 = 2
So 81411-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N4O/c6-4-3-5(10-9-4)8-2-1-7-3/h1-2H,(H2,6,9)

81411-79-2SDS

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 3-Aminoisoxazolo[4,5-b]pyrazine

1.2 Other means of identification

Product number -
Other names [1,2]oxazolo[4,5-b]pyrazin-3-amine

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:81411-79-2 SDS

81411-79-2Relevant academic research and scientific papers

A high-yielding method for the preparation of isoxazolopyridin-3-amine derivatives

Yu, Wensheng,Bulger, Paul G.,Maloney, Kevin M.

, p. 4941 - 4946 (2016/10/12)

A highly efficient and green method has been developed for the rapid preparation of highly functionalized isoxazolopyridin-3-amine derivatives in excellent yields. This process has a broad substrate scope, is operationally simple, and generally requires no chromatographic purification. In addition, the process is scalable and significantly greener than current alternatives with a PMI of 18 and water as the reaction solvent.

NEW SYNTHETIC APPROACH FOR PYRAZOLOPYRAZINES AND ISOXAZOLOPYRAZINES

Kocevar, Marjan,Tisler, Miha,Stanovnik, Branko

, p. 339 - 342 (2007/10/02)

A new synthetic approach has been developed for the synthesis of pyrazolepyrazines (7) and isoxazolopyrazines (22) from the corresponding substituted pyrazines.

Neighbouring Group Participation in Formation of Condensed Azines. Formation of Pyrazolo(3,4-b)pyrazines, Isoxazolo(4,5-b)pyrazines and Isothiazolo(5,4-b)pyridine (Heterocycles, CCX)

Kocevar, Marjan,Vercek, Bojan,Stanovnik, Branko,Tisler, Miha

, p. 731 - 744 (2007/10/02)

Pyrazine- and pyridinecarboxamidoximes with an amino, potentially tautomeric hydroxy or mercapto group in ortho position could be transformed in the appropriate condensed azines.In this manner, representatives of pyrazolo(3,4-b)pyrazine, isoxazolo(4,5-b)pyrazine and isothiazolo(5,4-b)pyridine ring system were synthesized and some transformations investigated. - Keywords: Cyclization with N-N, N-O or N-S bond formation; Heterocyclic compounds

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