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(E)-1-(2-iodophenyl)-3-p-tolylprop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1254271-38-9

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1254271-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254271-38-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,2,7 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1254271-38:
(9*1)+(8*2)+(7*5)+(6*4)+(5*2)+(4*7)+(3*1)+(2*3)+(1*8)=139
139 % 10 = 9
So 1254271-38-9 is a valid CAS Registry Number.

1254271-38-9Relevant academic research and scientific papers

Enantioselective Intramolecular Reductive Heck Reaction with a Palladium/Monodentate Phosphoramidite Catalyst

Mannathan, Subramaniyan,Raoufmoghaddam, Saeed,Reek, Joost N. H.,de Vries, Johannes G.,Minnaard, Adriaan J.

, p. 551 - 554 (2017)

A palladium-catalyzed enantioselective reductive Heck reaction of enones using monodentate phosphoramidite ligands is described. α,α,α’,α’-tetraaryl-1,3-dioxolane-4,5-dimethanol (TADDOL)-based phosphoramidites with palladium(II) acetate, and N-methyl dicy

Organocatalytic cascade reactions for multi-functionalized chiral cyclic ethers through vinylideneortho-quinone methides

Chang, Yu,Jia, Shiqi,Mao, Hui,Qin, Wenling,Tian, Yuhong,Wang, Pengfei,Yan, Hailong

supporting information, p. 11334 - 11337 (2021/11/09)

An organocatalytic approach to installing various alcohols into the carbonyl of α,β-unsaturated ketones mediated byVQMintermediates was achieved, followed by dearomatization to provide the stereo-defined cyclic ethersviaa cascade process. Along with the t

Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C-S Bond Formations Using Xanthate as Sulfur Source

Sangeetha, Subramani,Muthupandi, Pandi,Sekar, Govindasamy

, p. 6006 - 6009 (2016/01/09)

An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-bromochalco

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