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1H-Pyrazol-5-ol, 3-methyl-1-phenyl-, benzoate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56159-67-2

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56159-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56159-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,5 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56159-67:
(7*5)+(6*6)+(5*1)+(4*5)+(3*9)+(2*6)+(1*7)=142
142 % 10 = 2
So 56159-67-2 is a valid CAS Registry Number.

56159-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-methyl-1-phenyl-1H-pyrazol-5-yl) benzoate

1.2 Other means of identification

Product number -
Other names benzoic acid-(5-methyl-2-phenyl-2H-pyrazol-3-yl ester)

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:56159-67-2 SDS

56159-67-2Relevant academic research and scientific papers

Rapid microwave-enhanced synthesis of 1-phenyl-3-methyl-5-Acyloxypyrazoles under solvent-free conditions

Bai, Yinjuan,Lu, Jun,Gan, Haiying,Wang, Zhenjun

, p. 2549 - 2553 (2002)

The microwave-enhanced synthesis of 5-acyloxypyrazoles from 1-phenyl-3-methylpyrazole-5-one and acid chlorides under solvent-free conditions has been achieved in moderate to good yield.

Antioxidant and acetylcholinesterase inhibition activity of aliphatic and aromatic edaravone derivatives

Barajas-Carrillo, Victor Wagner,Estolano-Cobián, Arturo,Díaz-Rubio, Laura,Ayllón-Gutiérrez, Rocío Rosario,Salazar-Aranda, Ricardo,Díaz-Molina, Raúl,García-González, Víctor,Almanza-Reyes, Horacio,Rivero, Ignacio A.,Marrero, Joaquín G.,Córdova-Guerrero, Iván

, p. 610 - 623 (2020/11/24)

As Alzheimer disease (AD) is a multifactorial condition, it should be tackled with drugs targeting multiple key pathways. A series of aliphatic (2–8) and aromatic (9–15) edaravone derivatives were synthesized, characterized, and evaluated as antioxidant a

Synthesis of 1-acyl-1,2-dihydro-3H-pyrazol-3-ones via Lewis acid-mediated rearransement of 3-acyloxypyrazoles

Maruoka, Hiroshi,Yamagata, Kenji,Okabe, Fumi,Tomioka, Yukihiko

, p. 859 - 865 (2007/10/03)

The unusual formation of 1-acyl-1,2-dihydro-3H-pyrazol-3-ones starting from 3-acyloxypyrazoles by Fries-type rearrangement is described. Under normal conditions, acylation of 2,4-dihydro-3H-pyrazol-3-ones 1 and 2 with acid chlorides or anhydrides in the p

Structures of 1-Phenyl-3-methyl-pyrazolone-5- and its Benzoyl Derivatives

Okafor, Emmanuel Chukwuemeka

, p. 1019 - 1023 (2007/10/02)

The sturctures of 1-phenyl-3-methyl-pyrazolone-5 and its benzoyl derivatives have been investigated by means of IR, UV, NMR, and mass spectral spectroscopy. 1-Phenyl-3-methyl-pyrazolone-5-is found to exist as a zwitter ion in the solid state, in the 5-ket

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