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

73097-75-3

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73097-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73097-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,9 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 73097-75:
(7*7)+(6*3)+(5*0)+(4*9)+(3*7)+(2*7)+(1*5)=143
143 % 10 = 3
So 73097-75-3 is a valid CAS Registry Number.

73097-75-3SDS

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 4-acetyl-5-methyl-2-(4-methylphenyl)-4H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 3H-Pyrazol-3-one,4-acetyl-2,4-dihydro-5-methyl-2-(4-methylphenyl)

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:73097-75-3 SDS

73097-75-3Relevant academic research and scientific papers

Synthesis, crystal structural characterization and biological properties of thiosemicarbazones of schiff bases derived from 4-Acyl-2-pyrazoline-5-one

Rana, Arjunsinh,Parekh, Nayan,Dabhi, Harish,Bhoi, Dipak,Kumari, Niraj

experimental part, p. 1820 - 1831 (2012/06/01)

A novel synthesis, single crystal and biological activity of 4-acylthiosemicarbazone-3-methyl-1-(4'-methylphenyl)-2-pyrazolin-5-one by condensation of 4-acyl-3-methyl-1-(4'-methylphenyl)-2-pyrazolin-5-one with thiosemicarbazide was carried out. The compou

Synthesis and spectral characterization of Cu(II) complexes of some thio-Schiff bases of acyl pyrazolone analogues

Yadav, Ravindra J.,Vyas, Komal M.,Jadeja

experimental part, p. 1820 - 1831 (2010/11/03)

A series of tridentate pyrazolone-based thio-Schiff bases were synthesized by the interaction of 4-acyl/aroyl pyrazolones with thiosemicarbazide in an ethanolic medium. All of these ligands were characterized on the basis of elemental analysis, infrared (IR), 1H- and 13C-NMR data. Nuclear magnetic resonance (NMR) suggests the amine-one form of ligand in solution at room temperature. Copper Schiff-base complexes, [Cu(L)(H2O)], have been prepared by the interaction of the aqueous solution of copper sulfate pentahydrate with hot ethanolic solution of the appropriate ligand. The resulting complexes have been characterized by elemental analysis, metal content determination, molar conductance, fast atom bombardment mass spectra, magnetic measurements, thermogravimetric analysis (TGA), IR, and electronic spectral studies. Thermal stability, heat capacity, and activation energy of thermal degradation for these complexes were determined by TGA, differential thermal analysis, and differential scanning calorimetry. Suitable structures are proposed for these complexes.

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