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5731-13-5

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5731-13-5 Usage

Chemical Properties

White to cream solid

Check Digit Verification of cas no

The CAS Registry Mumber 5731-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5731-13:
(6*5)+(5*7)+(4*3)+(3*1)+(2*1)+(1*3)=85
85 % 10 = 5
So 5731-13-5 is a valid CAS Registry Number.

5731-13-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L06396)  4'-Ethylbiphenyl-4-carboxylic acid, 98%   

  • 5731-13-5

  • 1g

  • 616.0CNY

  • Detail

5731-13-5SDS

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-(4-Ethylphenyl)Benzoic Acid

1.2 Other means of identification

Product number -
Other names 4-(4-ETHYLPHENYL)BENZOIC ACID

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:5731-13-5 SDS

5731-13-5Relevant articles and documents

A comparative study of catalytic activity on iron-based carbon nanostructured catalysts with Pd loading: Using the Box–Behnken design (BBD) method in the Suzuki–Miyaura coupling

Moniriyan, Faezeh,Sabounchei, Seyyed Javad

, (2021/09/13)

Highly dispersed palladium nanoparticles immobilized on surface-modified Fe3O4 NPs and magnetic carbon nanostructures (CNSs; carbon nanotubes/graphene oxide) were synthesized and applied as a recyclable and reusable nanocatalyst to achieve palladium (II)-catalyzed Suzuki–Miyaura reaction of arylboronic acid with aryl bromides. Carbon nanostructures with immobilized hydantoin (PH)-Pd complex display excellent stability, including a high performance at low catalyst loading. Magnetic separation prevents catalyst centrifuge or filtration and also contributes to practical techniques for recovery. Next, a response surface method based on a three-level Box–Behnken design was used, which involved three factors: catalyst loading, reaction time, and solvent. The Box–Behnken method was advantageous to parameters optimization for obtaining a yield, with high efficiency and accuracy. As a result of catalytic tests, the TONs and TOFs were calculated from all coupling reactions. The prepared nano-magnetic catalysts, after the catalysis reaction, can be easily recovered through the magnetic field. Evaluated catalytic performance indicates that these types of catalysts can function as effective recyclable catalysts at least five times without losing the initial level of catalytic activity.

A highly efficient catalyst of a nitrogen-based ligand for the Suzuki coupling reaction at room temperature under air in neat water

Liu, Shiwen,Lv, Meiyun,Xiao, Daoan,Li, Xiaogang,Zhou, Xiuling,Guo, Mengping

supporting information, p. 4511 - 4516 (2014/06/23)

Glycine, as a kind of commercially available and inexpensive ligand, is used to prepare an air-stable and water-soluble catalyst for the Suzuki-Miyaura reaction in our study. In the presence of 0.1% [PdCl2(NH 2CH2COOH)2] as the catalyst, extremely excellent catalytic activity towards the Suzuki-Miyaura coupling of aryl halides containing the carboxyl group with various aryl boronic acids is observed at room temperature under air in neat water. the Partner Organisations 2014.

Four-coordinate Pd(II) complexes containing non-symmetric phosphorus ylides: Synthesis, characterization, and catalytic behavior towards Suzuki reaction

Sabounchei, Seyyed Javad,Panahimehr, Mohammad,Ahmadi, Mohsen,Nasri, Zahra,Khavasi, Hamid Reza

, p. 207 - 213 (2013/02/25)

In this paper it is reported the synthesis of the complexes of the type {[Ph2PCH2PPh2CHC(O)R]PdCl2} (R = 4′-biphenyl (1), OCH2Ph (2), 4-methylphenyl (3), 2-naphtyl (4), 2,4-dichlorophenyl (5), 3-nitro

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