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619-64-7

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619-64-7 Usage

Chemical Properties

white to beige powder

Uses

Different sources of media describe the Uses of 619-64-7 differently. You can refer to the following data:
1. 4-Ethylbenzoic acid was used in the synthesis of ethyl 4-vinyl-α-cyano-β-phenylcinnamate. It was also used to functionalize the edge of “pristine” graphite in the presence of polyphosphoric acid/phosphorus pentoxide.
2. Intermediates of Liquid Crystals

General Description

4-Ethylbenzoic acid reacts with lanthanum nitrate in aqueous solution to yield the polymer catena-poly[[aqua(4-ethylbenzoic acid-κO)lanthanum(III)]-tri-μ-4-ethylbenzoato].

Check Digit Verification of cas no

The CAS Registry Mumber 619-64-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 619-64:
(5*6)+(4*1)+(3*9)+(2*6)+(1*4)=77
77 % 10 = 7
So 619-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O2/c1-2-7-3-5-8(6-4-7)9(10)11/h3-6H,2H2,1H3,(H,10,11)/p-1

619-64-7 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A10235)  4-Ethylbenzoic acid, 99%   

  • 619-64-7

  • 10g

  • 347.0CNY

  • Detail
  • Alfa Aesar

  • (A10235)  4-Ethylbenzoic acid, 99%   

  • 619-64-7

  • 50g

  • 897.0CNY

  • Detail
  • Alfa Aesar

  • (A10235)  4-Ethylbenzoic acid, 99%   

  • 619-64-7

  • 250g

  • 3591.0CNY

  • Detail

619-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethylbenzoic Acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 4-ethyl-

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:619-64-7 SDS

619-64-7Relevant articles and documents

Carboxylation of sodium arylsulfinates with CO2over mesoporous K-Cu-20TiO2

Chen, Lei,Chen, Yanjiao,Dai, Xuan,Peng, Xinhua,Wu, Tao,Zhang, Wenwei

, p. 772 - 776 (2022/01/22)

A mesoporous ternary metal oxide (K-Cu-20TiO2) from a simple sol-gel method was prepared to catalyze heterogeneously the carboxylation reaction of various sodium arylsulfinates under atmospheric carbon dioxide. The catalyst showed excellent selectivity and good functional group tolerance to carboxylation recycle. The oxidation state of active copper(i) by characterization using FTIR, XRD, TG, XPS and TEM techniques proved to be efficacious to conduct atom economical reactions.

Photoredox-Catalyzed Simultaneous Olefin Hydrogenation and Alcohol Oxidation over Crystalline Porous Polymeric Carbon Nitride

Qiu, Chuntian,Sun, Yangyang,Xu, Yangsen,Zhang, Bing,Zhang, Xu,Yu, Lei,Su, Chenliang

, p. 3344 - 3350 (2021/07/26)

Booming of photocatalytic water splitting technology (PWST) opens a new avenue for the sustainable synthesis of high-value-added hydrogenated and oxidized fine chemicals, in which the design of efficient semiconductors for the in-situ and synergistic utilization of photogenerated redox centers are key roles. Herein, a porous polymeric carbon nitride (PPCN) with a crystalline backbone was constructed for visible light-induced photocatalytic hydrogen generation by photoexcited electrons, followed by in-situ utilization for olefin hydrogenation. Simultaneously, various alcohols were selectively transformed to valuable aldehydes or ketones by photoexcited holes. The porosity of PPCN provided it with a large surface area and a short transfer path for photogenerated carriers from the bulk to the surface, and the crystalline structure facilitated photogenerated charge transfer and separation, thus enhancing the overall photocatalytic performance. High reactivity and selectivity, good functionality tolerance, and broad reaction scope were achieved by this concerted photocatalysis system. The results contribute to the development of highly efficient semiconductor photocatalysts and synergistic redox reaction systems based on PWST for high-value-added fine chemical production.

A Zn(II)-Coordination Polymer for the Instantaneous Cleavage of Csp3-Csp3 Bond and Simultaneous Reduction of Ketone to Alcohol

Das, Gourab Kanti,Dey, Biswajit,Dhibar, Subhendu,Ghosh, Debasish,Gupta, Vivek K.

, (2020/04/10)

Two coordination polymers of Zn(II) and Cu(II) with n-butylmalonic acid have been achieved in this work. The crystallographic structural descriptions along with the sedimentary rock-type microstructural morphology of these two coordination polymers (CPs) have been explored. The reactivity of β-hydroxy ketones with these two CPs has also been investigated. The Zn(II)-CP shows a specific reactivity with β-hydroxy ketone at room temperature and in open air conditions. Through a microcolumn-based filtration technique, the Zn(II)-CP shows the capability to break the Csp3-Csp3 σ bonds of β-hydroxy ketone and simultaneously reduce the associated ketone to alcohol. Such conversion has been progressed without the use of any additional external reducing agent and any chemical workup or column chromatographic purification protocol. Other similar type CPs of Cu(II) and Mn(II) with n-butylmalonic acid completely failed to show similar reactivity with β-hydroxy ketone. On the basis of much experimental evidence, the most possible mechanistic pathway of the reactivity between β-hydroxy ketone and Zn(II)-CP has also been proposed through this work.

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