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4-Butyryl-3-methyl-1-phenyl-2-pyrazolin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22616-35-9

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22616-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22616-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,1 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22616-35:
(7*2)+(6*2)+(5*6)+(4*1)+(3*6)+(2*3)+(1*5)=89
89 % 10 = 9
So 22616-35-9 is a valid CAS Registry Number.

22616-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butanoyl-5-methyl-2-phenyl-4H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-methyl-4-butyryl-2-pyrazolin-5-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:22616-35-9 SDS

22616-35-9Relevant academic research and scientific papers

Chelation and extraction of copper(II) with 5-pyrazolone-based Schiff bases

Parmar,Barad,Pansuriya,Patel

experimental part, p. 688 - 698 (2011/12/16)

Copper(II) chelates of the Schiff bases (H2L), obtained by condensation of 4-butyryl-3-methyl-1-phenyl-pyrazoline-5-one (HBMPP) with o-phenylene diamine (H2L1) and p-phenylene diamine (H 2L2), have be

Neutral dioxovanadium(V) complexes of biomimetic hydrazones ONO donor ligands of bioinorganic and medicinal relevance: Synthesis via air oxidation of bis(acetylaceto-nato)oxovanadium(IV), characterization, biological activity and 3D molecular modeling

Maurya,Rajput

, p. 133 - 144 (2008/10/09)

The interaction of bis(acetylacetonato)oxovanadium(IV), [VO(acac)2] with biomimetic hydrazone ONO donor ligands HL in 1:1 mole ratio [where, HL = N-(4′-benzoylidene-3′-methyl-1′-phenyl-2′-pyrazolin-5′-one)-isonicotinic acid hydrazide (bmphp-inH, I), N-(4′-butyrylidene-3′-methyl-1′-phenyl-2′-pyrazolin-5′-one)-isonicotinic acid hydrazide (bumphp-inH, II), N-(4′-acetylidene-3′-methyl-1′-phenyl-2′-pyrazolin-5′-one)-isonicotinic acid hydrazide (amphp-inH, III), N-(3′-methyl-1′-phenyl-4′-propionylidene-2′-pyrazolin-5′-one)-isonicotinic acid hydrazide (mphpp-inH, IV) and N-(4′-iso-butyrylidene-3′-methyl-1′-phenyl-2′-pyrazolin-5′-one)-isonicotinic acid hydrazide (iso-bumphp-inH, V)] in a mixed solvent (ethanol-methanol, 1:10) via aerial oxidation for 2-3 days yield dioxovanadium(V) complexes of composition [VO2(L)(H2O)] · H2O. The compounds so obtained were characterized on the basis of elemental analyses, thermogravimetry, vanadium determination, IR, Electronic, 51V NMR, 1H NMR and mass spectral studies. The 3D molecular modeling and analysis for bond lengths and bond angles have also been carried out for one of the representative compounds, [VO2(ampph-in)(H2O)] (3).

Physicochemical studies of symmetrical tetradentate schiff base complexes of chromium(III), cobalt(II), nickel(II), copper(II), zinc(II), oxovanadium(IV) and dioxouranium(VI) derived from 4-acyl pyrazolone and 1,4-diamine

Thaker,Patel,Lekhadia,Thaker

, p. 483 - 488 (2007/10/03)

A few symmetrical tetradentate schiff base (TSB) complexes of the type [M(TSB)], [where M = Cr(III), Co(II), Ni(II), Cu(II), Zn(II), Vo(II) and UO2(II); TSB derived from 4-acyl pyrazolone (4-acyl = 4-propionyl or 4-butyryl) and 1,4-butylene dia

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