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2-Propen-1-one, 3-phenyl-1-(2-quinolinyl)-, also known as 3-phenyl-1-(2-quinolyl)-2-propen-1-one, is a chemical compound with the molecular formula C18H13NO. It is a derivative of 2-propen-1-one, featuring a phenyl group at the 3-position and a 2-quinolinyl group at the 1-position. 2-Propen-1-one, 3-phenyl-1-(2-quinolinyl)- is an organic molecule with potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to note that handling and usage of this chemical should be done with caution, as it may have specific safety and health considerations.

1033-74-5

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1033-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1033-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1033-74:
(6*1)+(5*0)+(4*3)+(3*3)+(2*7)+(1*4)=45
45 % 10 = 5
So 1033-74-5 is a valid CAS Registry Number.

1033-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1-quinolin-2-ylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-phenyl-1-quinolin-2-yl-propenone

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:1033-74-5 SDS

1033-74-5Downstream Products

1033-74-5Relevant academic research and scientific papers

Synthesis of Stereoprojecting, Chiral N-C(sp3)-E Type Pincer Complexes

Balázs, László B.,Tay, Wee Shan,Li, Yongxin,Pullarkat, Sumod A.,Leung, Pak-Hing

, p. 2272 - 2285 (2018)

A synthetic strategy to generate chiral N-C(sp3)-E (E = S, O) pincer complexes incorporating enhanced stereoprojecting groups at the N-arm site has been established. The synthesis of the tridentate pincer ligand was carried out via palladacycle-catalyzed asymmetric hydrophosphination of N-chelating enones. The chelation properties of the substrates were initially demonstrated on C(sp2)-N type palladacycles. The extended substrate scope allows versatile structural modifications on the ligand backbone. Subsequent cyclometalation provided N-C(sp3)-E complexes in a diastereoselective reaction.

Fabrication of Copper-based Silica-coated Magnetic Nanocatalyst for Efficient One-pot Synthesis of Chalcones via A3 Coupling of Aldehydes-Alkynes-Amines

Yadav, Priya,Yadav, Manavi,Gaur, Rashmi,Gupta, Radhika,Arora, Gunjan,Rana, Pooja,Srivastava, Anju,Sharma, Rakesh K.

, p. 2488 - 2496 (2020/03/26)

In the present work, we have synthesized bioactive and pharmacologically important chalcone motifs by employing green and efficient silica-coated magnetically separable catalyst, Cu@DBM@ASMNPs. The highly proficient nanocatalyst proves its invincibility f

Microwave assisted one pot three component synthesis of propargylamine, tetra substituted propargylamine and pyrrolo[1,2-: A] quinolines using CuNPs@ZnO-PTh as a heterogeneous catalyst

Shah, Akshara P.,Sharma, Anuj S.,Jain, Shilpa,Shimpi, Navinchandra G.

, p. 8724 - 8737 (2018/06/08)

The present work deals with the investigation and catalytic activity analysis of copper nanoparticles (CuNPs) supported on a zinc oxide-polythiophene (ZnO-PTh) nanocomposite. CuNPs@ZnO-PTh was prepared using a simple impregnation method and characterized

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