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536-66-3

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536-66-3 Usage

Description

4-Isopropylbenzoic acid, also known as cuminic acid, is a white crystalline powder that is a derivative of benzoic acid with an isopropyl group substitution at the 4th position. It is a cumic acid characterized by its distinct chemical properties and potential applications in various industries.

Uses

Used in Chemical Synthesis:
4-Isopropylbenzoic acid is used as a key intermediate in the synthesis of various organic compounds, particularly in the production of triorganotin carboxylates with different substituents at the tin atom. These synthesized products are fully characterized by spectroscopic and thermal techniques, providing insights into the coordination number of the tin atom in both solution and solid state.
Used in Pharmaceutical Industry:
4-Isopropylbenzoic acid, due to its unique chemical structure, can be utilized in the development of pharmaceutical compounds. Its potential applications in drug discovery and design can contribute to the creation of novel therapeutic agents for various medical conditions.
Used in Material Science:
The white crystalline nature of 4-Isopropylbenzoic acid makes it a candidate for use in the development of new materials with specific properties. Its incorporation into various formulations can lead to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 536-66-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 536-66:
(5*5)+(4*3)+(3*6)+(2*6)+(1*6)=73
73 % 10 = 3
So 536-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)

536-66-3 Well-known Company Product Price

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  • Alfa Aesar

  • (B20704)  4-Isopropylbenzoic acid, 99%   

  • 536-66-3

  • 5g

  • 554.0CNY

  • Detail
  • Alfa Aesar

  • (B20704)  4-Isopropylbenzoic acid, 99%   

  • 536-66-3

  • 25g

  • 1724.0CNY

  • Detail
  • Alfa Aesar

  • (B20704)  4-Isopropylbenzoic acid, 99%   

  • 536-66-3

  • 100g

  • 5834.0CNY

  • Detail

536-66-3SDS

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 p-cumic acid

1.2 Other means of identification

Product number -
Other names 4-Isopropylbenzoic 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:536-66-3 SDS

536-66-3Relevant articles and documents

Ogan

, p. 2823 (1971)

An efficient chromium(iii)-catalyzed aerobic oxidation of methylarenes in water for the green preparation of corresponding acids

Jiang, Feng,Liu, Shanshan,Wei, Yongge,Yan, Likai,Yu, Han,Zhao, Wenshu

supporting information, p. 12413 - 12418 (2021/09/28)

A highly efficient method to oxidize methylarenes to their corresponding acids with a reusable Cr catalyst was developed. The reaction can be carried out in water with 1 atm oxygen and K2S2O8as cooxidants, proceeds under green and mild conditions, and is suitable for the oxidation of both electron-deficient and electron-rich methylarenes, including heteroaryl methylarenes, even at the gram level. The excellent result, together with its simplicity of operation and the ability to continuously reuse the catalyst, makes this new methodology environmentally benign and cost-effective. The generality of this methodology gives it the potential for use on an industrial scale. Differing from the accepted oxidation mechanism of toluene, GC-MS studies and DFT calculations have revealed that the key benzyl alcohol intermediate is formed under the synergetic effect of the chromium and molybdenum in the Cr catalyst, which can be further oxidized to afford benzaldehyde and finally benzoic acid.

Palladium supported on a novel ordered mesoporous polypyrrole/carbon nanocomposite as a powerful heterogeneous catalyst for the aerobic oxidation of alcohols to carboxylic acids and ketones on water

Ganji, Nasim,Karimi, Babak,Najafvand-Derikvandi, Sepideh,Vali, Hojatollah

, p. 13616 - 13631 (2020/04/24)

Preparation of an ordered mesoporous polypyrrole/carbon (PPy/OMC) composite has been described through a two-step nanocasting process using KIT-6 as a template. Characterization of the PPy/OMC nanocomposite by various analysis methods such as TEM, XRD, TGA, SEM and N2 sorption confirmed the preparation of a material with ordered mesoporous structure, uniform pore size distribution, high surface area and high stability. This nanocomposite was then used for the immobilization of palladium nanoparticles. The nanoparticles were almost uniformly distributed on the support with a narrow particle size of 20-25 nm, confirmed by various analysis methods. Performance of the Pd?PPy/OMC catalyst was evaluated in the aerobic oxidation of various primary and secondary alcohols on water as a green solvent, giving the corresponding carboxylic acids and ketones in high yields and excellent selectivity. The catalyst could also be reused for at least 10 reaction runs without losing its catalytic activity and selectivity. High catalytic efficiency of the catalyst can be attributed to a strong synergism between the PPy/OMC and that of supported Pd nanoparticles.

Cobalt-Catalyzed Acceptorless Dehydrogenation of Alcohols to Carboxylate Salts and Hydrogen

Gunanathan, Chidambaram,Kishore, Jugal,Pattanaik, Sandip,Pradhan, Deepak Ranjan

supporting information, (2020/03/03)

The facile oxidation of alcohols to carboxylate salts and H2 is achieved using a simple and readily accessible cobalt pincer catalyst (NNNHtBuCoBr2). The reaction follows an acceptorless dehydrogenation pathway and displays good functional group tolerance. The amine-amide metal-ligand cooperation in cobalt catalyst is suggested to facilitate this transformation. The mechanistic studies indicate that in-situ-formed aldehydes react with a base through a Cannizzaro-type pathway, resulting in potassium hemiacetolate, which further undergoes catalytic dehydrogenation to provide the carboxylate salts and H2

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