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2,3-Dihydro-2,3-bis(4-methylphenyl)-1,4-phthalazinedione, also known as DIBMP, is a chemical compound characterized by a phthalazine backbone. It presents as a yellow crystalline powder that is insoluble in water but readily soluble in organic solvents. 2,3-Dihydro-2,3-bis(4-methylphenyl)-1,4-phthalazinedione is recognized for its utility in various chemical processes due to its unique structural properties.

63546-89-4

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63546-89-4 Usage

Uses

Used in Organic Synthesis:
2,3-Dihydro-2,3-bis(4-methylphenyl)-1,4-phthalazinedione is used as a reducing agent in organic synthesis for its ability to facilitate chemical reactions, particularly in the reduction of other compounds, which is essential for the production of a variety of organic molecules.
Used in Dye and Pigment Production:
In the dye and pigment industry, 2,3-Dihydro-2,3-bis(4-methylphenyl)-1,4-phthalazinedione serves as a dye intermediate, contributing to the creation of a spectrum of colorants and pigments that are used in various applications, including textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
2,3-Dihydro-2,3-bis(4-methylphenyl)-1,4-phthalazinedione is utilized in the pharmaceutical sector for the synthesis of diverse pharmaceutical compounds, playing a crucial role in the development of new drugs and medicines.
Given its low toxicity and relative safety when handled with appropriate precautions, DIBMP is a valuable compound in the realms of chemical manufacturing and research.

Check Digit Verification of cas no

The CAS Registry Mumber 63546-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 63546-89:
(7*6)+(6*3)+(5*5)+(4*4)+(3*6)+(2*8)+(1*9)=144
144 % 10 = 4
So 63546-89-4 is a valid CAS Registry Number.

63546-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(4-methylphenyl)phthalazine-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,3-di-p-tolyl-2,3-dihydro-phthalazine-1,4-dione

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:63546-89-4 SDS

63546-89-4Downstream Products

63546-89-4Relevant academic research and scientific papers

Electrochemical Conversion of Phthaldianilides to Phthalazin-1,4-diones by Dehydrogenative N?N Bond Formation

Kehl, Anton,Gieshoff, Tile,Schollmeyer, Dieter,Waldvogel, Siegfried R.

, p. 590 - 593 (2018)

The electrochemical synthesis of 6-membered rings via anodic dianilide N?N coupling is challenging due to concurring benzoxazole co-formation. The rigidity of the a phthalic acid backbone allows a novel access to phthalazin-1,4-diones by N?N bond formation using anodically generated amidyl radicals. Since conventional synthetic routes to phthalazin-1,4-diones require the use of toxic N,N′-diarylhydrazines and generate reagent waste, a safer and more sustainable approach is required. Easy accessible starting materials, a broad scope of applicable functional groups, promising yields, and a very simple set-up elevate this sustainable method.

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