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3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-2-phenyl-4-(2-thienylcarbonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

29665-05-2

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29665-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29665-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,6 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29665-05:
(7*2)+(6*9)+(5*6)+(4*6)+(3*5)+(2*0)+(1*5)=142
142 % 10 = 2
So 29665-05-2 is a valid CAS Registry Number.

29665-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-phenyl-4-(thiophene-2-carbonyl)-4H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 1-phenyl-3-methyl-4-thienoylpyrazol-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:29665-05-2 SDS

29665-05-2Downstream Products

29665-05-2Relevant academic research and scientific papers

Mixed-ligand lanthanide complexes with acylpyrazolones and phosphorus-containing ligands

Belousov,Drozdov,Verteletskii,Prishchenko,Livantsova,Novikova

, p. 278 - 282 (2013)

The reactions of lanthanum acetylacetonate with various phosphorus-containing pesticides, toxic gases, and products of their hydrolysis are modeled by quantum-chemical methods. In the most cases, the enthalpy of substitution for water by organophosphorus

The reactivity of new (1,5-cyclooctadiene)rhodium acylpyrazolonates towards N- and P-donor ligands: X-ray structures of [Rh(1,5-COD)Qs], [Rh(1,5-COD)(phen)]Qs·0.5H2O (HQs=1-phenyl-3-methyl-4-(2-thenoyl)-pyrazol-5-one) and [Rh(1,5-COD)Br]2

Pettinari, Claudio,Marchetti, Fabio,Cingolani, Augusto,Bianchini, Gianluca,Drozdov, Andrei,Vertlib, Vyacheslav,Troyanov, Sergei

, p. 5 - 14 (2002)

Complexes [Rh(1,5-COD)(Q)] have been prepared by the reaction between [Rh(1,5-COD)Cl]2 (1,5-COD=1,5-cyclooctadiene) and HQ (where HQ=1-phenyl-3-methyl-4-R-pyrazol-5-one: R=2-thenoyl (HQs), 2-furanoyl (HQo) or tert-butylacetyl (HQT). [Rh(1,5-COD)(Q)] react with N2-donor ligands such as 1,10-phenanthroline (phen) or 2,2-bipyridyl (bipy) yielding ionic compounds [Rh(1,5-COD)(N2 -donor)]Q. The substitutional lability of 1,5-COD in [Rh(1,5-COD)(Q)] versus mono- and di-organophosphine ligands was also investigated. In all cases 1,5-COD has been displaced. Reaction with two equivalents of PPh3 gave, upon oxidation of the Rh(I) centre, [Rh(PPh3)2(O2)(Q)] species containing a η2-peroxo-group. Reaction of [Rh(1,5-COD)(Q)] with the chelating P2-donor 1,2-bis(diphenylphosphino)ethane (dppe) or 4,4′-bis(diphenylphosphino)ferrocene (dppf) yields the peroxo Rh(III) compounds [Rh(dppe)2O2]QT and [Rh(dppf)O2(Qs)] or Rh(I) species [Rh(dppf-O2)(QT)] containing the diphosphine in the oxidised form. Finally the reaction between [Rh(1,5-COD)(Q)] and allylbromide yields the well-known [Rh(1,5-COD)Br]2. All complexes have been characterised by analytical and spectral data (IR, 1H and 31P{1H}-NMR spectra). The crystal structures of [Rh(1,5-COD)(Qs)], [Rh(1,5-COD)(phen)]Qs and [Rh(1,5-COD)Br2, all containing a Rh(I) atom in a square coordinate environment, are also reported.

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