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4-Formylphenyl benzoate is an organic compound with the chemical formula C14H10O3. It is a derivative of benzoic acid, featuring a benzene ring with a formyl group (aldehyde) at the 4-position and an ester group connecting it to another benzene ring. This white crystalline solid is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the production of dyes, fragrances, and polymers. The compound is characterized by its melting point of 95-97°C and is soluble in common organic solvents. Due to its reactivity, it is essential to handle 4-formylphenyl benzoate with care, following proper safety protocols.

5339-06-0

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5339-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5339-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5339-06:
(6*5)+(5*3)+(4*3)+(3*9)+(2*0)+(1*6)=90
90 % 10 = 0
So 5339-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O3/c15-10-11-6-8-13(9-7-11)17-14(16)12-4-2-1-3-5-12/h1-10H

5339-06-0SDS

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 (4-formylphenyl) benzoate

1.2 Other means of identification

Product number -
Other names 4-Benzoyloxy-benzaldehyd

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:5339-06-0 SDS

5339-06-0Relevant articles and documents

Synthesis, Electronic Spectroscopy, Cyclic Voltammetry, Photophysics, Electrical Properties and X-ray Molecular Structures of meso-{Tetrakis[4-(benzoyloxy)phenyl]porphyrinato}zinc(II) Complexes with Aza Ligands

Nasri, Soumaya,Zahou, Imen,Turowska-Tyrk, Ilona,Roisnel, Thierry,Loiseau, Fredérique,Saint-Amant, Eric,Nasri, Habib

, p. 5004 - 5019 (2016)

The synthesis of the new meso-porphyrin tetrakis[4-(benzoyloxy)phenyl]porphyrin (H2TPBP), the meso-{tetrakis[4-(benzoyloxy)phenyl]porphyrinato}zinc(II) starting material [Zn(TPBP)] (1), and the 1,4-diazabicyclo[2.2.2]octane (dabco), pyrazine (pyz), 4,4′-bipyridine (4,4′-bpy), 4,4′-diaminodiphenylmethane (4,4′-mda), and 4-cyanopyridine (4-CNpy) coordination compounds with [Zn(TPBP)] (2–7) are described. The preparation of the dabco derivative in chlorobenzene leads to a crystalline monomeric five-coordinate zinc porphyrin species (2), whereas the synthesis in dichloromethane gives a five-coordinate zinc metalloporphyrin dimer (3) in the solid state. The pyrazine derivative crystallizes as a bis-pyrazine six-coordinate zinc metalloporphyrin (4). Complex 5 in the solid state is a dimer with 4,4′-bpy as a bridging ligand, whereas the 4,4′-mda species (6) is a five-coordinated monomeric zinc derivative in the solid state. All of structures of 2–6 possess cavities with different dimensions in which solvent molecules are located. The solution UV/Vis spectra of 2–7 exhibit redshifted Soret bands that indicate that these derivatives are five-coordinate zinc(II) porphyrin complexes in solution. UV/Vis titrations show that the association constants of 2–7 are close to those of known five-coordinate zinc(II) meso-porphyrins. The1H NMR spectra of these species confirm this deduction. The photophysical proprieties of 1–7 are similar to those of related zinc(II) meso-porphyrins. The cyclic voltammograms of the H2TPBP free base and 1–7 present a third one-electron reversible oxidation wave. Single-layer diode devices of the [iridium tin oxide/zinc porphyrin/aluminum] configuration show relatively low turn-on voltages.

Green synthesis of some new thiopyrano[2,3-d][1,3]thiazoles using lemon juice and their antibacterial activity

Metwally, Nadia Hanafy,Badawy, Mohamed Ahmed,Okpy, Doha Samir

, p. 2496 - 2509 (2018)

A simple green method has been developed for the synthesis of a series of new 3-phenyl-6-(substituted)-thiopyrano[2,3-d]thiazole-2,5,7(6H)-triones, 6-cyano-2-oxo-3-phenyl-thiopyrano[2,3-d]thiazoles, 3-phenyl-3,5,5a,11b-tetrahydro-2H,6H-chromeno-[4′,3′:4,5

Electrochemical Aerobic Oxidative Cleavage of (sp3)C-C(sp3)/H Bonds in Alkylarenes

Liu, Shuai,Liu, Zhong-Quan,Shen, Tong,Shen, Xu,Wang, Nengyong,Wu, Jintao,Yang, Le,Zhao, Jianyou

, p. 3286 - 3295 (2022/03/14)

An electrochemistry-promoted oxidative cleavage of (sp3)C-C(sp3)/H bonds in alkylarenes was developed. Various aryl alkanes can be smoothly converted into ketones/aldehydes under aerobic conditions using a user-friendly undivided cell setup. The features of air as oxidant, scalability, and mild conditions make them attractive in synthetic organic chemistry.

PEROVSKITES FOR PHOTOCATALYTIC ORGANIC SYNTHESIS

-

, (2022/01/07)

Nature is capable of storing solar energy in chemical bonds via photosynthesis through a series of C—C, C—O and C—N bond-forming reactions starting from CO2 and light. Direct capture of solar energy for organic synthesis is a promising approach

Functionalized heterocycle-appended porphyrins: Catalysis matters

Abdulaeva, Inna A.,Birin, Kirill P.,Gorbunova, Yulia G.,Polivanovskaia, Daria A.,Tsivadze, Aslan Yu

, p. 42388 - 42399 (2020/12/09)

The scope and limitations of the condensation of labile 2,3-diaminoporphyrin derivatives with aromatic aldehydes to provide functionalized imidazole- and pyrazine-appended porphyrins were investigated in detail. The presence of an acidic catalyst in the reaction was found to be a tool that allows the reaction path to be switched. The influence of the electronic origin of the substituents in the carbonyl components of the condensation on the yields and selectivity of the reaction was revealed. Metal-promoted cross-coupling transformations were found to be convenient for the further targeted construction of functional derivatives based on the prepared bromo-substituted pyrazinoporphyrins. Overall, these strategies provide a versatile technique for the elaboration of a variety of functionalized heterocycle-appended porphyrins for further application in the development of hybrid materials. This journal is

New imidazolone derivatives comprising a benzoate or sulfonamide moiety as anti-inflammatory and antibacterial inhibitors: Design, synthesis, selective COX-2, DHFR and molecular-modeling study

Metwally, Nadia Hanafy,Mohamed, Mona Said

, (2019/12/12)

New imidazol-5-one derivatives 12a,b and 12e, f, 14a,b and 16a,b were synthesized and screened for their in vivo anti-inflammatory activity using a standard acute carrageenan-induced rat paw oedema method. All the tested compounds exhibited good anti-infl

Anti-Markovnikov hydroazidation of activated olefins via organic photoredox catalysis

Nicewicz, David A.,Onuska, Nicholas P. R.,Rosario Collazo, José L.,Schutzbach-Horton, Megan E.

supporting information, p. 55 - 59 (2019/12/30)

Organic azides serve as synthetically useful surrogates for primary amines, a functional group which is ubiquitous in bioactive and medicinally relevant molecules. Historically, the formal hydroazidation of simple activated olefins and styrenes has proven

Palladium-catalyzed aryloxy- and alkoxycarbonylation of aromatic iodides in γ-valerolactone as bio-based solvent

Tukacs, József M.,Marton, Bálint,Albert, Eszter,Tóth, Imre,Mika, László T.

, (2020/08/11)

Fossil-based solvents and triethylamine as a toxic and volatile base were successfully replaced with γ-valerolactone as a non-volatile solvent and K2CO3 as inorganic base in the alkoxy- and aryloxycarbonylation of aryl iodides using phosphine-free Pd catalyst systems. By this, the traditional systems were not simply replaced but also significantly improved. In the study, the effects of different reaction parameters, i.e. the use of several other solvents, the temperature, the carbon monoxide pressure, the base and the catalyst concentrations, were evaluated in details on the efficiency of the carbonylations. To gather some information on the mechanism of these reactions, the effects of the electronic parameters (σ) of various aromatic substituents of the aryl iodides as well as the influence of para-substitution of phenol were investigated on the activity. For a comparison, the aryl-substituted aryl iodides were also reacted with methanol and aryl iodide was also alkoxycarbonylated using several different lower alcohols. From the observed correlations between the electronic parameters of the aromatic substituents and the rates, it appears that the rate determining step is the oxidative addition of Ar–I to Pd0, provided that sufficient amounts of nucleophiles are present for the ester formation. If this is not the case, the rate of nucleophile attack might determine the overall rate.

Palladium-Catalyzed Aerobic Oxidative Coupling of Amides with Arylboronic Acids by Cooperative Catalysis

Li, Yue,Wu, Hongxiang,Zeng, Zhuo

supporting information, p. 4357 - 4361 (2019/07/09)

The first fluoride and palladium co-catalyzed conversion of amide to ester through an aerobic oxidative coupling pathway is reported. This new approach presents a practical process that employs easily available oxygen and commercially available arylboronic acids as coupling partners, uses a wide range of N- tosylamides, and proceeds under mild reaction conditions. This protocol demonstrates broad functional group tolerance, and provides an alternative option to synthesize esters from N-tosylamides which obtained by simply N-functionalization of secondary amides.

Oxidative coupling of tetraalkynyltin with aldehydes leading to alkynyl ketones

Levashov, Andrey S.,Aksenov, Nicolai A.,Aksenova, Inna V.,Konshin, Valeriy V.

, p. 8297 - 8304 (2017/08/14)

The reaction of tetraalkynyltin with aldehydes was studied for the first time. The reaction was shown to proceed as a tandem process of nucleophilic addition of tin acetylide to aldehyde followed by Oppenauer-type oxidation of produced tin alcoholates, an

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