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5,8-dichloropyrazino[2,3-d]pyridazine is a heterocyclic organic compound characterized by a molecular formula of C6H2Cl2N4. It features a pyrazine ring fused with a pyridazine ring, with chlorine atoms attached at the 5th and 8th positions. This unique structure and chemical properties make it a valuable building block for the synthesis of various organic compounds and a promising candidate for applications in the pharmaceutical and materials science industries.

13480-43-8

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13480-43-8 Usage

Uses

Used in Pharmaceutical Industry:
5,8-dichloropyrazino[2,3-d]pyridazine is used as a key intermediate in the development of new drugs and medications. Its unique structure allows for the creation of novel compounds with potential therapeutic effects.
Used in Materials Science:
5,8-dichloropyrazino[2,3-d]pyridazine is used as a component in the development of novel materials with specific electronic or optical properties. Its chemical properties and structure may contribute to the creation of materials with enhanced performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13480-43-8 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 13480-43:
(7*1)+(6*3)+(5*4)+(4*8)+(3*0)+(2*4)+(1*3)=88
88 % 10 = 8
So 13480-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl2N4/c7-5-3-4(6(8)12-11-5)10-2-1-9-3/h1-2H

13480-43-8SDS

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 5,8-Dichloropyrazino[2,3-d]pyridazine

1.2 Other means of identification

Product number -
Other names Pyrazino[2,3-d]pyridazine,5,8-dichloro

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:13480-43-8 SDS

13480-43-8Downstream Products

13480-43-8Relevant academic research and scientific papers

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

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

, (2021/05/31)

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.

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