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[1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis a heterocyclic chemical compound with the molecular formula C12H7N3S. It is characterized by the presence of both nitrogen and sulfur atoms in its structure, which contributes to its interesting chemical properties and potential biological activities. [1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis often utilized in organic synthesis and medicinal chemistry due to its versatility and the presence of the phenyl group, making it a valuable building block for the synthesis of various organic molecules.

112230-76-9

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112230-76-9 Usage

Uses

Used in Pharmaceutical Industry:
[1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis used as a key intermediate in the development of pharmaceutical drugs. Its unique structure and properties make it a promising candidate for the creation of new medications with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical industry, [1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis used as a component in the synthesis of agrochemicals. Its incorporation into these products can enhance their effectiveness in protecting crops from pests and diseases, ultimately contributing to increased agricultural productivity.
Used in Materials Science:
[1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis also utilized in materials science for the development of new materials with specific properties. Its unique chemical structure allows it to be incorporated into various materials, potentially leading to advancements in areas such as electronics, energy storage, and advanced materials for industrial applications.
Overall, [1,2,5]Thiadiazolo[3,4-b]pyrazine, 5-phenylis a versatile compound with a range of potential applications in different scientific and industrial fields, making it an important compound for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 112230-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,3 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112230-76:
(8*1)+(7*1)+(6*2)+(5*2)+(4*3)+(3*0)+(2*7)+(1*6)=69
69 % 10 = 9
So 112230-76-9 is a valid CAS Registry Number.

112230-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-[1,2,5]thiadiazolo[3,4-b]pyrazine

1.2 Other means of identification

Product number -
Other names [1,2,5]Thiadiazolo[3,4-b]pyrazine,5-phenyl

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:112230-76-9 SDS

112230-76-9Downstream Products

112230-76-9Relevant academic research and scientific papers

Studies on Pyrazines. Part 33.1 Synthesis of 2,3-Diaminopyrazines via [1,2,5]Thiadiazolo[3,4-b] pyrazines

Sato, Nobuhiro,Mizuno, Hajime

, p. 250 - 251 (1997)

The syntheses of [1,2,5]thiadiazolo[3,4-b]pyrazine (3) and its methyl and/or phenyl derivatives as well as their reduction to 2,3-diaminopyrazines 4 are described.

Electrochemical Properties of Pyrazinothiadiazoles

Camilleri, Patrick,Odell, Barbara,O'Neill, Peter

, p. 1671 - 1674 (2007/10/02)

The reduction properties of some pyrazinothiadiazoles have been measured by cyclic voltammetry and pulse radiolysis.Variation in substitution on the pyrazine ring has given compounds with half-peak reduction potentials varying betwee -280 and -1100 mV (versus Ag-AgCl) in 3:1 methanol-water.Some of these compounds act as Photosystem I electron acceptors at a concenmtration lower than 10-6 mol dm-3.MNDO calculations have been used to help in the understanding of the redox processes involving this class of molecules.

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