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6-benzoyl-2,5-diphenylpyridazin-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75872-31-0

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75872-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75872-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75872-31:
(7*7)+(6*5)+(5*8)+(4*7)+(3*2)+(2*3)+(1*1)=160
160 % 10 = 0
So 75872-31-0 is a valid CAS Registry Number.

75872-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-benzoyl-2,5-diphenylpyridazin-3-one

1.2 Other means of identification

Product number -
Other names 6-Benzoyl-2,5-diphenyl-3(2H)-pyridazinon

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:75872-31-0 SDS

75872-31-0Downstream Products

75872-31-0Relevant academic research and scientific papers

N-Heterocyclic Carbene-Catalyzed Oxidative Annulations of α,β-Unsaturated Aldehydes with Hydrazones: Selective Synthesis of Optically Active 4,5-Dihydropyridazin-3-ones and Pyridazin-3-ones

Mao, Jian-Hui,Wang, Zi-Tian,Wang, Zhan-Yong,Cheng, Ying

, p. 6350 - 6359 (2015)

A novel and efficient method for the highly enantioselective synthesis of chiral 4,5-dihydropyridazin-3-one derivatives has been developed based on the chiral N-heterocyclic carbene-catalyzed oxidative annulation between α,β-unsaturated aldehydes and hydrazones. Meanwhile, the selective synthesis of either 4,5-dihydropyridazin-3-ones or pyridazin-3-one derivatives from the same reactants has been achieved by simply varying catalytic and reaction conditions.

Reaction of triethyl phosphonoacetate anion with phenylhydrazones: A new method for the preparation of 3(2H)-pyridazinones

Patel,Vyas,Pandey,Tavares,Fernandes

, p. 1021 - 1026 (2007/10/02)

Various 5,6-disubstituted-2-phenyl-3(2H)-pyridazinones 4 have been synthesised by reacting triethyl phosphonoacetate anion with monophenylhydrazone of 1,2-dicarbonyl compounds 2.

A new and convenient synthesis of 3(2H)-pyridazinones by reacting carbanion of ethyl trimethylsilylacetate with phenylhydrazones

Patel,Vyas,Pandey,Tavares,Fernandes

, p. 1935 - 1940 (2007/10/02)

A one-pot synthesis of 5,6-disubstituted-2-phenyl-3(2H)-pyridazinones 4 is achieved on treatment of carbanion of ethyl trimethylsilylacetate with phenylhydrazones of 1,2-dicarbonyl compounds 1.

Cumulated Ylides, XIV - Phosphacumulene Ylides - Building Blocks for the Synthesis of Heterocyclic Compounds

Bestmann, Hans Juergen,Schmid, Guenter,Sandmeier, Dieter,Schade, Gerold,Oechsner, Helmut

, p. 1709 - 1719 (2007/10/02)

Phosphacumulene ylides 1 and acidic compounds 4 combine to give phosphoranes 5, which cyclize by an intramolecular reaction (mostly Wittig reaction) with formation of heterocycles 7.

Stickstoff- und Schwefelheterocyclen aus NH- und SH-aciden Carbonylverbindungen und Phosphacumulenyliden

Bestmann, Hans Juergen,Schmid, Guenter,Sandmeier, Dieter

, p. 2939 - 2942 (2007/10/02)

Phosphacumulenylide reagieren mit 1,2,3-Tricarbonyl-2-phenylhydrazonen zu Pyridazinderivaten, mit β-Ketoenaminen zu Pyridindionabkoemmlingen und mit α-Ketothiocarbonsaeureamiden zu Verbindungen der Dihydrothiophendion-Reihe.

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