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1,4-Phthalazinedione, 2,3-dihydro-2-methyl-3-phenyl-, also known as 2-methyl-3-phenyl-1,4-naphthoquinone, is an organic compound with the chemical formula C15H12O2. It is a derivative of phthalazinedione, featuring a naphthoquinone structure with a methyl group at the 2-position and a phenyl group at the 3-position. This yellow crystalline solid is used as an intermediate in the synthesis of various dyes and pigments, particularly those with anthraquinone structures. The compound is also known for its potential applications in the pharmaceutical industry, where it may be used as a building block for the development of new drugs. Its chemical properties and reactivity make it a valuable component in the creation of complex organic molecules.

89811-41-6

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89811-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89811-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89811-41:
(7*8)+(6*9)+(5*8)+(4*1)+(3*1)+(2*4)+(1*1)=166
166 % 10 = 6
So 89811-41-6 is a valid CAS Registry Number.

89811-41-6SDS

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 2-methyl-3-phenylphthalazine-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-methyl-3-phenyl-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:89811-41-6 SDS

89811-41-6Downstream Products

89811-41-6Relevant academic research and scientific papers

INHIBITORS OF IRES-MEDIATED PROTEIN SYNTHESIS

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Page/Page column 38; 45; 46, (2017/12/18)

This disclosure relates to inhibitors of IRES-mediated protein synthesis, compositions comprising therapeutically effective amounts of these compounds, and methods of using those compounds and compositions in treating hyperproliferative disorders, e.g., cancers. This disclosure also relates to compositions comprising inhibitors of IRES-mediated protein synthesis and mTOR inhibitors, and to methods of treating cancer by conjoint administration of inhibitors of IRES-mediated protein synthesis and mTOR inhibitors.

REACTION OF AMINONITRENES WITH AZO COMPOUNDS. I. REACTION OF PHTHALIMIDONITRENE WITH ALKANEAZOBENZENES

Kuznetsov, M. A.,Suvorov, A. A.

, p. 2260 - 2269 (2007/10/02)

The reaction of phthalimidonitrene with the simplest alkaneazobenzenes leads to the formation of pairs of stereoisomeric 2-alkyl-3-phenyl-1-phthalimidoazimines differing in the configuration at the N2N3 bond; the isomeric 3-alkyl-2-phenyl-1-phthalimidoazimines were not found in the reaction mixtures.The individual stereoisomers of the 2-alkyl-3-phenyl-1-phthalimidoazimines are stable in the solid state at room temperature, but in solutions they are slowly converted into an equilibrium mixture of the isomers; when heated, they release nitrogen with the formation of 2-alkyl-3-phenyl-2,3-dihydrophthalazine-1,4-diones.

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