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2-(2-Hydroxyethyl)-6-phenyl-3(2H)-pyridazinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23916-77-0

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23916-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23916-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,1 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23916-77:
(7*2)+(6*3)+(5*9)+(4*1)+(3*6)+(2*7)+(1*7)=120
120 % 10 = 0
So 23916-77-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2/c15-9-8-14-12(16)7-6-11(13-14)10-4-2-1-3-5-10/h1-7,15H,8-9H2

23916-77-0SDS

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 2-(2-hydroxyethyl)-6-phenylpyridazin-3-one

1.2 Other means of identification

Product number -
Other names 3(2H)-Pyridazinone,2-(2-hydroxyethyl)-6-phenyl

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:23916-77-0 SDS

23916-77-0Relevant academic research and scientific papers

Arylpiperazinylalkyl-3(2-H)-pyridazinones

-

, (2008/06/13)

A description is given of new arylpiperazinylalkyl-3(2H)-pyridazinones of general formula (I) and their preparation and their addition salts with pharmaceutically acceptable acids, in which R1is a methyl or phenyl radical, R2is a hyd

Substituted 6-phenyl-3(2H)-pyridazinones useful as cardiotonic agents

-

, (2008/06/13)

Substituted 6-phenyl-3(2H)-pyridazinone compounds are useful as cardiotonic agents. Said compounds cause a significant increase in myocardial contractility in the anesthetized dog. Said compounds are produced by reacting substituted γ-oxobenzenebutanoic acids with suitably substituted hydrazines to provide 6-phenyl-4,5-dihydro-3(2H)-pyridazinones which are dehydrogenated to the desired product. The intermediate 6-phenyl-4,5-dihydro-3(2H)-pyridazinones are themselves useful as cardiotonic agents.

Pyridazinones. 3. Synthesis, Antisecretory, and Antiulcer Activities of 2-Cyanoguanidine Derivatives

Yamada, Toshihiro,Shimamura, Hiroshi,Tsukamoto, Yoshitsugu,Yamaguchi, Azuma,Ohki, Masahiko

, p. 1144 - 1149 (2007/10/02)

3(2H)-Pyridazinone derivatives having a 2-cyanoguanidine moiety, as well as a sulfur or an oxygen atom in the alkylene side chain, were synthesized and evaluated for gastric antisecretory and antiulcer activities.The key intermediates, free amines having

VINYLATION OF 3-PYRIDAZONES

Shatalov, G.V.,Gridchin, S.A.,Mikhant'ev, B.I.

, p. 299 - 302 (2007/10/02)

The vinylation of 3-pyridazones through a step involving the production of 2-hydroxy- and 2-chloroethyl-substituted compounds with subsequent dehydrochlorination, as well as vinylation by means of vinyl acetate, in all cases leads only to N-vinyl derivati

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