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Ethyl 4-(4-nitrophenyl)benzoate is a chemical compound belonging to the benzoate esters family. It is a yellow, crystalline solid with a molecular formula of C15H13NO4 and a molecular weight of 271.26 g/mol. Ethyl 4-(4-nitrophenyl)benzoate is characterized by the presence of a nitro group in its structure, which makes it an important intermediate for the synthesis of various organic compounds. Ethyl 4-(4-nitrophenyl)benzoate is widely used in the field of organic chemistry as a reagent for different synthetic reactions and is also utilized in the production of pharmaceuticals, fragrances, and other chemical products. As with all chemicals, proper handling and safety precautions should be observed when working with Ethyl 4-(4-nitrophenyl)benzoate.

6242-99-5

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6242-99-5 Usage

Uses

Used in Organic Chemistry:
Ethyl 4-(4-nitrophenyl)benzoate is used as a reagent in organic chemistry for various synthetic reactions. Its unique structure and the presence of the nitro group make it a valuable intermediate for the synthesis of diverse organic compounds.
Used in Pharmaceutical Industry:
Ethyl 4-(4-nitrophenyl)benzoate is used as an intermediate in the production of pharmaceuticals. Its versatile chemical properties allow it to be incorporated into the synthesis of various drug molecules, contributing to the development of new medications.
Used in Fragrance Industry:
Ethyl 4-(4-nitrophenyl)benzoate is used as a component in the production of fragrances. Its unique chemical structure contributes to the creation of distinct scents and aromas, enhancing the variety of fragrances available in the market.
Used in Chemical Product Industry:
Ethyl 4-(4-nitrophenyl)benzoate is utilized in the production of various chemical products. Its versatility and reactivity make it a valuable component in the synthesis of a wide range of chemical products, including dyes, plastics, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 6242-99-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6242-99:
(6*6)+(5*2)+(4*4)+(3*2)+(2*9)+(1*9)=95
95 % 10 = 5
So 6242-99-5 is a valid CAS Registry Number.

6242-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4'-nitro-[1,1'-biphenyl]-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-(4-nitrophenyl)benzoate

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:6242-99-5 SDS

6242-99-5Relevant academic research and scientific papers

Palladium/tris(tert-butyl)phosphine-catalyzed Suzuki cross-couplings in the presence of water

Lou, Sha,Fu, Gregory C.

supporting information; experimental part, p. 2081 - 2084 (2010/10/20)

Dipalladiumtris(dibenzylideneacetone)/tris(tert-butyl)phosphonium tetrafluoroborate/potassium fluoride dihydrate [Pd2(dba) 3/[HP(t-Bu)3]BF4/KF·2H2O] serves as a mild, robust, and user-friendly method for the efficient Suzuki cross-coupling of a diverse array of aryl and heteroaryl halides with aryl- and heteroarylboronic acids.

Use of functionalized onium salts as a soluble support for organic synthesis

-

Page/Page column 51-52, (2010/11/25)

The invention relates to the use of a onium salt functionalized by at least one organic function, as a soluble support, in the presence of at least one organic solvent, for organic synthesis of a molecule, in a homogenous phase, by at least one transformation of said organic function. The onium salt enables the synthesized molecule to be released. The onium salt is present in liquid or solid form at room temperature and corresponds to formula A1+, X1?, wherein A1+ represents a cation and X1? represents an anion.

Polymer-Assisted Solution-Phase (PASP) Suzuki Couplings Employing an Anthracene-Tagged Palladium Catalyst

Lan, Ping,Berta, Daniela,Porco Jr., John A.,South, Michael S.,Parlow, John J.

, p. 9678 - 9686 (2007/10/03)

A general method for polymer-assisted solution-phase (PASP) Suzuki reactions employing a combination of anthracene-tagged palladium catalyst and anthracene-tagged boronic acid with a polymer-supported carbonate base is reported. The anthracene-tagged catalyst allows for the easy removal of the Pd catalyst along with the dissociated phosphine ligand and phosphine oxide byproducts by sequestration through a chemoselective Diels-Alder reaction with a maleimide resin. The polymer-supported carbonate base facilitates the removal of excess boronic acid and the borane-containing byproducts present at the end of the coupling reaction. The Suzuki coupling reaction can be efficiently conducted by using combinations of the anthracene-tagged Pd catalyst, polymer-supported carbonate base, and anthracene-tagged boronic acid to yield the desired product in high purity and yield without the use of chromatography.

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