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13480-40-5

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13480-40-5 Usage

Description

6,7-Dihydropyrazino[2,3-d]pyridazine-5,8-dione is a complex fused heterocyclic chemical compound characterized by the presence of both pyrazine and pyridazine rings. 6,7-DIHYDROPYRAZINO[2,3-D]PYRIDAZINE-5,8-DIONE features a dione functional group, which endows it with potential reactivity and biological activity. Its structural complexity and pharmacological properties have attracted attention in the scientific community, making it a promising candidate for drug target research. The synthesis and exploration of its potential biological activities are subjects of ongoing research, with applications in medicinal chemistry and pharmaceutical research as a potential scaffold for new drug development.

Uses

Used in Pharmaceutical Research:
6,7-Dihydropyrazino[2,3-d]pyridazine-5,8-dione is used as a potential drug scaffold for the development of new pharmaceuticals due to its unique structural features and potential biological activity. Its complex ring system and dione functional group offer opportunities for the design of novel therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6,7-Dihydropyrazino[2,3-d]pyridazine-5,8-dione serves as a promising starting point for the synthesis of new compounds with potential therapeutic applications. Its structural complexity allows for various modifications and functionalizations, enabling the exploration of its pharmacological properties and the optimization of its biological activity.
Note: Since the provided materials do not specify particular applications or industries for 6,7-Dihydropyrazino[2,3-d]pyridazine-5,8-dione, the uses listed above are general and based on the compound's potential in pharmaceutical research and medicinal chemistry. Further research and development may reveal specific applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 13480-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13480-40:
(7*1)+(6*3)+(5*4)+(4*8)+(3*0)+(2*4)+(1*0)=85
85 % 10 = 5
So 13480-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N4O2/c11-5-3-4(6(12)10-9-5)8-2-1-7-3/h1-2H,(H,9,11)(H,10,12)

13480-40-5SDS

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 6,7-dihydropyrazino[2,3-d]pyridazine-5,8-dione

1.2 Other means of identification

Product number -
Other names 1,2,3,4-Tetrahydro-2,3,5,8-tetrazanaphthalin-1,4-dion

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:13480-40-5 SDS

13480-40-5Relevant articles and documents

Structural identification between phthalazine-1,4-diones and n-aminophthalimides via vilsmeier reaction: Nitrogen cyclization and tautomerization study

Chung, Cheng-Yen,Li, Sin-Min,Lin, Hui-Yi,Tsai, Shuo-En,Tseng, Ching-Chun,Wong, Fung Fuh

, (2021)

N-aminophthalimides and phthalazine 1,4-diones were synthesized from isobenzofuran1,3-dione, isoindoline-1,3-dione, furo [3,4-b] pyrazine-5,7-dione, or 1H-pyrrolo [3,4-c] pyridine-1,3dione with monohydrate hydrazine to carry out the 5-exo or 6-endo nitrogen cyclization under the different reaction conditions. Based on the control experimental results, 6-endo thermodynamic hydrohydrazination and kinetical 5-exo cyclization reactions were individually selective formation. Subsequently, Vilsmeier amidination derivatization was successfully developed to probe the structural divergence between N-aminophthalimide 2 and phthalazine 1,4-dione 3. On the other hand, the best tautomerization of N-aminophthalimide to diazinone was also determined under acetic acid mediated solution.

Heterocyclic Analogues of Phthalhydrazides: Cyclic Hydrazides of Pyridine 1-Oxide and Pyrazine 1,4-Dioxide Dicarboxylic Acids

Paul, D. Brenton

, p. 87 - 94 (2007/10/02)

The synthesis of N-oxides of the cyclic hydrazides of pyridine and pyrazine o-dicarboxylic acids is described.Pyridopyridazine-5,8-dione 1-oxide, pyridopyridazine-1,4-dione 6-oxide, and pyrazinopyridazine-5,8-dione 1,2-dioxide, were obtained by direct oxidation of the parent hydrazides with peracetic acid.The pyridopyridazine derivatives were also unambiguously synthesized by treating the anhydrides or diesters of the relevant carboxylic acid 1-oxides with hydrazine hydrate.

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