Welcome to LookChem.com Sign In|Join Free
  • or
6-acetyl-5-methyl-2-phenylpyridazin-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75872-28-5

Post Buying Request

75872-28-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

75872-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75872-28-5 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75872-28:
(7*7)+(6*5)+(5*8)+(4*7)+(3*2)+(2*2)+(1*8)=165
165 % 10 = 5
So 75872-28-5 is a valid CAS Registry Number.

75872-28-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-acetyl-5-methyl-2-phenylpyridazin-3-one

1.2 Other means of identification

Product number -
Other names 6-acetyl-5-methyl-2-phenylpyridazin-3(2H)-one

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:75872-28-5 SDS

75872-28-5Relevant academic research and scientific papers

Microwaves in organic synthesis: Facile synthesis of biologically active pyridazinone and iminopyridazine derivatives

Mohamed, Nadia Ragab,El-Saidi, Manal Mohamed Talaat,Ali, Yasser Mahmoud,Elnagdi, Mohamed Hilmy

, p. 1333 - 1337 (2008/09/18)

(Chemical Equation Presented) Condensation of Wittig reagents 1a,b with arylhydrazones 2a,b by conventional and by microwave heating techniques furnished the corresponding pyridazines 3a-e. The arylhydrazones 7a,b were allowed to react with 1a,b under the same conditions to produce the pyridazinones 10a,b and iminopyridazines 11a,b respectively. On the other hand, the arylhydrazones 12a-c reacted with 1a to afford the pyridazinones 13a-c. Treatment of 3b with dimethylformamide dimethyl acetal (DMFDMA) produced the adduct 15. The utility of microwave heating technique led to the reduction of the reaction times to few minutes and to the improvement of the yields of the products. The in vitro biological activity of some newly prepared compounds against four types of fungi was studied.

The Utility of Phosphonium Ylides in Heterocyclic Synthesis: Synthesis of Pyridazinone and tetrahydrocinnolinone Derivatives

Nada, Afaf Aly,Erian, Ayman Wahba,Mohamed, Nadia Ragab,Mahran, Asma Mohamed

, p. 1576 - 1594 (2007/10/03)

The synthesis of pyridazinone and tetrahydrocinnolinone derivatives via the reaction of phosphonium ylides with different hydrazones was accomplished.The reaction of Wittig reagents with a pyridazinone derivative was also achieved. - Keywords: phosphonium ylides; hydrazones; pyridazinones and tetrahydrocinnolinones

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.

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.

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 75872-28-5