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1H-Pyrazole, 5-(3-chlorophenyl)-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16860-57-4

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16860-57-4 Usage

Class

Organic compounds

Subclass

Phenylpyrazoles

Specific family

Diphenylpyrazole

Structure

Pyrazole ring attached to two phenyl groups

Chlorophenyl group location

5-position (3-chlorophenyl)

Potential hazards

Toxic (handle with caution)

Uses

Pharmaceutical and research purposes

Studied in

Scientific fields for properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 16860-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16860-57:
(7*1)+(6*6)+(5*8)+(4*6)+(3*0)+(2*5)+(1*7)=124
124 % 10 = 4
So 16860-57-4 is a valid CAS Registry Number.

16860-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-chlorophenyl)-1,3-diphenylpyrazole

1.2 Other means of identification

Product number -
Other names 5-(m-Chlorphenyl)-1,3-diphenylpyrazol

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:16860-57-4 SDS

16860-57-4Downstream Products

16860-57-4Relevant academic research and scientific papers

Photooxidation of 3,5-diaryl-1-phenyl-2-pyrazolines: Experimental and computational studies

Soltani, Marzieh,Memarian, Hamid Reza,Sabzyan, Hassan

, (2019/12/23)

Photooxidation of various 2-pyrazolines is studied experimentally and computationally. Experimental results show that the electron-donating/withdrawing substituents increases/decreases the rate of this photoreaction. The proposed light-induced electron-tr

Silica-supported 1,3-dichloro-5,5-dimethylhydantoin (DCH) as a useful reagent for microwave-assisted aromatization of 1,3,5-trisubstituted pyrazolines under solvent-free conditions

Azarifar, Davood,Nadimi, Elahe,Ghanbari, Mohammd Mehdi

experimental part, p. 447 - 450 (2012/02/01)

1,3,5-Trisubstituted pyrazolines are rapidly and conveniently oxidized to their corresponding pyrazoles by 1,3-dichloro-5,5-dimethylhydantoin (DCH) in solution and solvent-free conditions under microwave irradiation. The presence of silica gel as a suppor

Aromatization of 1,3,5-trisubstituted of 4,5-dihydro-1H-pyrazoles by in-situ generation of I+ from hydrogen Peroxide/Acids/iodide potassium or sodium systems

Maleki, Behrooz,Veisi, Hojat

experimental part, p. 4366 - 4370 (2012/02/16)

A simple, green and cost-effective protocol was used for the aromatization of 1,3,5-trisubstituted-2-pyrazolines to the corresponding pyrazoles by in situ generation of iodine (I+) from H2O2/AcOH or SSA or oxalic acid /KI

A convenient and efficient protocol for the synthesis of 5-aryl-1,3-diphenylpyrazole catalyzed by hydrochloric acid under ultrasound irradiation

Li, Ji-Tai,Yin, Ying,Li, Ling,Sun, Ming-Xuan

experimental part, p. 11 - 13 (2010/11/16)

The synthesis of 5-aryl-1,3-diphenylpyrazole via the reactions of 3-aryl-2,3-epoxy-1-phenyl-1-propanone with phenylhydrazine was carried out in 69-99% yields at room temperature under ultrasound irradiation. This method provides several advantages such as

An efficient oxidation of 2-pyrazolines and isoxazolines by bis-bromine-1,4-diazabicyclo[2.2.2]octane complex (DABCO-Br2)

Azarifar, Davood,Khosravi, Kaveh,Veisi, Rahman-Ali

experimental part, p. 178 - 184 (2010/10/03)

An efficient and simple procedure has been developed for the oxidation of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles and -isoxazoles to their corresponding aromatic derivatives promoted by bis-bromine-1,4-diazabicyclo[2.2. 2]octane complex (DABCO-Brsu

Solvent-free synthesis of 1, 3-diphenyl-5-arylpyrazole derivatives

Li, Ji-Tai,Yin, Ying,Meng, Xian-Tao

experimental part, p. 384 - 386 (2010/04/23)

The synthesis of 1, 3-diphenyl-5-arylpyrazoles via the reactions of 2, 3-epoxy-1-phenyl-3-aryl-1-propanones with phenylhydrazine was carried out in 48-84% yields at 230 °C under solvent-free condition within 1.5 h. This method provides several advantages

Oxidative aromatization of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles efficiently by tetrabromine-1,3,5,7-tetrazatricyclo[3.3.1.13,7]decane complex, Br4-TATCD, as a novel reagent both under microwave irradiation and at room temper

Azarifar, Davood,Khosravi, Kaveh

experimental part, p. 43 - 46 (2010/04/05)

Oxidation of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles to the corresponding pyrazoles has been achieved by utilizing tetrabromine-1,3,5,7-tetrazatricyclo[3.3.1.13,7]decane complex, Br4-TATCD, in glacial acetic acid under microwav

Silica sulfuric acid-activated poly-1,3-dichloro-5methyl-5-(4'-vinylphenyl)hydantoin (PDCVH) as an effective reagent for oxidation of 1,3,5-trisubstituted 2-pyrazolines both under microwave irradiation and thermal conditions

Azarifar, Davood,Maleki, Behrooz,Setayeshnazar, Mehrnaz

, p. 669 - 673 (2008/09/20)

Oxidation of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles to the corresponding pyrazoles has been achieved by utilizing silica sulfuric acidactivated poly-1,3-dichloro-5-methyl-5(4'-vinylphenyl)hydantoin in EtOH under both microwave irradiation and conve

Microwave-promoted oxidation of 1,3,5-trisubstituted 4,5-dihydro-1H- pyrazoles by in-situ generation of NO+ and NO2+ respectively from sodium nitrite and sodium nitrate in acetic acid

Azarifar, Davood,Maleki, Behrooz,Sahraei, Mahta

, p. 563 - 565 (2008/09/19)

(Chemical Equation Presented) Microwave-assisted aromatization of 1,3,5-trisubstituted 4,5-dihydro-1H-pyrazoles by in-situ generation of NO + and NO2+ respectively from sodium nitrite and sodium nitrate in acetic acid has

Microwave-assisted aromatization of 1,3,5-trisubstituted 2-pyrazolines by Bi(NO3)3 · 5H2O, as a novel and convenient oxidizing agent

Azarifar, Davood,Maleki, Behrooz

, p. 2581 - 2585 (2007/10/03)

Bismuth(III) nitrate pentahydrate, Bi(NO3)3 · 5H2O, has been used as a mild, efficient, and inexpensive oxidant for the oxidative aromatization of several 1,3,5-trisubstituted 2-pyrazolines to pyrazoles in acetic acid unde

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