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2-cyclohexyl-3-hydroxy-3-phenyl-2,3-dihydro-1H-isoindol-1-one is a cycloalkylphenol compound belonging to the class of isoindolones. It features a cyclic structure with a hydroxyl group attached to the cyclohexyl ring and a phenyl group connected to the isoindolone ring. This chemical compound has potential applications in the pharmaceutical industry due to its possible biological activities and pharmacological properties, which warrant further research to explore its full potential.
Used in Pharmaceutical Industry:
2-cyclohexyl-3-hydroxy-3-phenyl-2,3-dihydro-1H-isoindol-1-one is used as a potential pharmaceutical candidate for drug development due to its potential biological activities and pharmacological properties. Its cycloalkylphenol structure and the presence of a hydroxyl group and phenyl group may contribute to its therapeutic effects, making it a compound of interest for further research and development in the pharmaceutical field.

3593-38-2

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3593-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3593-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3593-38:
(6*3)+(5*5)+(4*9)+(3*3)+(2*3)+(1*8)=102
102 % 10 = 2
So 3593-38-2 is a valid CAS Registry Number.

3593-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyclohexyl-3-hydroxy-3-phenylisoindol-1-one

1.2 Other means of identification

Product number -
Other names 2-cyclohexyl-3-hydroxy-3-phenyl-2,3-dihydro-isoindol-1-one

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:3593-38-2 SDS

3593-38-2Downstream Products

3593-38-2Relevant academic research and scientific papers

Eosin Y as a Redox Catalyst and Photosensitizer for Sequential Benzylic C?H Amination and Oxidation

Yan, Dong-Mei,Zhao, Quan-Qing,Rao, Li,Chen, Jia-Rong,Xiao, Wen-Jing

, p. 16895 - 16901 (2018/10/26)

A new synergistic multicatalytic activation mode of eosin Y has been discovered by exploiting the redox potential of its ground state and excited state. This catalytic strategy proves to be an enabling tool for visible-light-driven sequential benzylic C?H amination and oxidation of o-benzyl-N-methoxyl-benzamides when using Selectfluor as a hydrogen atom transfer (HAT) reagent and O2 as oxidant. Efficient synthesis of a range of diversely functionalized 3-hydroxyisoindolinones can thus be achieved with good yields and selectivity at mild reaction conditions. Preliminary mechanistic studies and DFT calculations suggest that eosin Y works as a redox catalyst and photosensitizer.

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