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56052-53-0

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56052-53-0 Usage

General Description

3-(2-hydroxyphenyl)-1-phenylpropan-1-one is a chemical compound with the molecular formula C15H14O2. It is a ketone that consists of a central phenyl ring attached to a three-carbon chain with a hydroxyphenyl group and a phenyl ring attached at different positions. This chemical is commonly used in organic synthesis and pharmaceutical research due to its versatile reactivity and potential biological activity. It has been studied for its potential applications in the development of new drugs and as a building block for the synthesis of complex molecules. Additionally, its unique structure and properties make it an important molecule in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 56052-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,5 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56052-53:
(7*5)+(6*6)+(5*0)+(4*5)+(3*2)+(2*5)+(1*3)=110
110 % 10 = 0
So 56052-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O2/c16-14-9-5-4-8-13(14)10-11-15(17)12-6-2-1-3-7-12/h1-9,16H,10-11H2

56052-53-0SDS

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 3-(2-hydroxyphenyl)-1-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3-(2-hydroxy-phenyl)-1-phenyl-propan-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:56052-53-0 SDS

56052-53-0Relevant articles and documents

Chemoselective transfer hydrogenation of Α,Β-unsaturated carbonyls catalyzed by a reusable supported Pd nanoparticles on biomass-derived carbon

Song, Tao,Duan, Yanan,Yang, Yong

, p. 80 - 85 (2019/01/03)

We herein report highly chemoselective transfer hydrogenation of α,β-unsaturated carbonyl compounds to saturated carbonyls with formic acid as a hydrogen donor over a stable and recyclable heterogeneous Pd nanoparticles (NPs) on N,O-dual doped hierarchical porous biomass-derived carbon. The synergistic effect between Pd NPs and incorporated heteroatoms on carbon plays a critical role on promoting the reaction efficiency. A series of α,β-aromatic and aliphatic unsaturated carbonyl compounds was selectively reduced to their corresponding saturated carbonyls in up to 97% isolated yields with good tolerance of various functional groups. In addition, the catalyst can be successively reused for at least 6 times without significant loss in reaction efficiency.

One-Pot Synthesis of O-Heterocycles or Aryl Ketones Using an InCl3/Et3SiH System by Switching the Solvent

Jia, Wenqiang,Xi, Qiumu,Liu, Tianqi,Yang, Minjian,Chen, Yonghui,Yin, Dali,Wang, Xiaojian

, p. 5141 - 5149 (2019/05/10)

An efficient one-pot synthesis of O-heterocycles or aryl ketones has been achieved using Et3SiH in the presence of InCl3 via a sequential ionic hydrogenation reaction by switching the solvent. This methodology can be used to construct C-O bonds and to prepare conjugate reduction products, including chromans, tetrahydrofurans, tetrahydropyrans, dihydroisobenzofurans, dihydrochalcones, and 1,4-diones in a facile manner. In addition, a novel plausible mechanism involving a conjugate reduction and a tandem reductive cyclization was verified by experimental investigations.

Nanopalladium on polyethylenimine–grafted starch: An efficient and ecofriendly heterogeneous catalyst for Suzuki–Miyaura coupling and transfer hydrogenation reactions

Fu, Lixia,Deng, Wenxiu,Liu, Lujie,Peng, Yanqing

, (2017/10/06)

Functionalized natural polysaccharides are attractive supports for colloidal metal nanocatalysts due to their abundance, cheapness, biocompatibility and biodegradability. In this study, isocyanate–functionalized starch was prepared by treating with diisocyanate. Polyethylenimine grafted onto starch via the formation of urea linker. The palladium nanoparticles deposited starch PEIS@Pd(0) was obtained through a chelating–in situ reduction procedure. Characterization of these materials was done using Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, X–ray diffraction, and inductive coupled plasma atomic emission spectrometry. The catalytic activity of PEIS@Pd(0) was then tested in two series of model reactions: Suzuki–Miyaura coupling and transfer hydrogenation. The catalyst could be recovered by simple filtration and was reused for five times without significant loss of catalytic activity, which confirmed the good stability of the catalyst.

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