Welcome to LookChem.com Sign In|Join Free
  • or
4,5-Dihydro-6-(1-Methylethyl)-3(2H)-Pyridazinone, also known as disodium pyridazinone, is a pyridazinone derivative with the molecular formula C8H12N2O. It is a chemical compound that possesses anti-inflammatory and analgesic properties, making it a promising candidate for pharmaceutical applications.

210230-80-1

Post Buying Request

210230-80-1 Suppliers

Recommended suppliers

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

210230-80-1 Usage

Uses

Used in Pharmaceutical Industry:
4,5-Dihydro-6-(1-Methylethyl)-3(2H)-Pyridazinone is used as a therapeutic agent for its potential to reduce pain and inflammation. It is being studied for its role in treating conditions such as arthritis and migraines, where its anti-inflammatory and analgesic properties can provide relief to patients.
Used in Drug Development:
4,5-Dihydro-6-(1-Methylethyl)-3(2H)-Pyridazinone is utilized in the development of new medications to explore its potential benefits in treating various inflammatory and painful conditions. Ongoing research aims to further understand its mechanisms of action and optimize its use as a pharmaceutical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 210230-80-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,2,3 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 210230-80:
(8*2)+(7*1)+(6*0)+(5*2)+(4*3)+(3*0)+(2*8)+(1*0)=61
61 % 10 = 1
So 210230-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N2O/c1-5(2)6-3-4-7(10)9-8-6/h5H,3-4H2,1-2H3,(H,9,10)

210230-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-propan-2-yl-4,5-dihydro-1H-pyridazin-6-one

1.2 Other means of identification

Product number -
Other names PYR065

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:210230-80-1 SDS

210230-80-1Relevant academic research and scientific papers

Further studies on 2-arylacetamide pyridazin-3(2H)-ones: Design, synthesis and evaluation of 4,6-disubstituted analogs as formyl peptide receptors (FPRs) agonists

Giovannoni, Maria Paola,Schepetkin, Igor A.,Cilibrizzi, Agostino,Crocetti, Letizia,Khlebnikov, Andrei I.,Dahlgren, Claes,Graziano, Alessia,Dal Piaz, Vittorio,Kirpotina, Liliya N.,Zerbinati, Serena,Vergelli, Claudia,Quinn, Mark T.

, p. 512 - 528 (2013/07/27)

Formyl peptide receptors (FPRs) play an essential role in the regulation of endogenous inflammation and immunity. In the present studies, a large series of pyridazin-3(2H)-one derivatives bearing an arylacetamide chain at position 2 was synthesized and te

FUSED HETEROCYCLIC SULFONYLUREA COMPOUND, HERBICIDE CONTAINING THE SAME, AND METHOD OF CONTROLLING WEED WITH THE SAME

-

Page 23, (2010/02/08)

The present invention provides a compound represented by the formula: wherein Q represents a fused heterocyclic group, X and Y are the same or different and each represent an optionally halogenated lower alkyl group, an optionally halogenated lower alkoxy group, etc. , or a salt thereof, as well as a herbicide comprising the compound or a salt thereof, which exhibits a significant effect for control of sulfonylurea herbicide-resistant weeds in paddy fields and can reduce the number of active ingredients in a combined preparation and a method of controlling sulfonylurea herbicide-resistant weeds which comprises using the same.

An efficient approach to γ-alkylidene γ-butyrolactones: Application to the syntheses of pyridazinones and diazocinones

Reddy, Ravinder S.,Saravanan,Kumar, Pradeep

, p. 6553 - 6564 (2007/10/03)

The efficient phototransformation of a variety of spirodiones 3 to γ- alkylidene γ butyrolactones 4 and their application to the syntheses of biologically useful pyridazinones 14 and diazocinones 15 are described.

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 210230-80-1