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4-methylphenyl 3-iodoprop-2-yn-1-yl ether is an organic chemical compound characterized by its unique structure and properties. It features a 4-methylphenyl group, which is a benzene ring with a methyl group attached at the 4th position, and a 3-iodoprop-2-yn-1-yl ether group, which consists of a propargyl ether with an iodine atom at the 3rd position. 4-methylphenyl 3-iodoprop-2-yn-1-yl ether is known for its potential applications in the synthesis of various organic molecules and pharmaceuticals, particularly in the area of radiopharmaceuticals due to the presence of the iodine atom. The compound's structure allows for versatile chemical reactions, making it a valuable intermediate in organic synthesis.

4269-46-9

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4269-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4269-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,6 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4269-46:
(6*4)+(5*2)+(4*6)+(3*9)+(2*4)+(1*6)=99
99 % 10 = 9
So 4269-46-9 is a valid CAS Registry Number.

4269-46-9Downstream Products

4269-46-9Relevant academic research and scientific papers

Copper-mediated trifluoromethylation of 5-iodotriazole with (trifluoromethyl)trimethylsilane promoted by silver carbonate

Fu, Dan,Zhang, Jian,Cao, Song

, p. 170 - 176 (2013/11/19)

A novel and mild method for copper-mediated trifluoromethylation of 5-iodotriazole using (trifluoromethyl)trimethylsilane (Me3SiCF 3) as trifluoromethylating reagent with the assistance of Ag 2CO3 was developed.

Synthesis of organochalcogen propargyl aryl ethers and their application in the electrophilic cyclization reaction: An efficient preparation of 3-halo-4-chalcogen-2H-benzopyrans

Godoi, Benhur,Speranca, Adriane,Back, Davi F.,Brandao, Ricardo,Nogueira, Cristina W.,Zeni, Gilson

supporting information; body text, p. 3469 - 3477 (2009/09/06)

We herein described the synthesis of various organochalcogen propargyl aryl ethers via reaction of lithium acetylide intermediate with electrophilic chalcogen (sulfur, selenium, tellurium) species. Various aryl and alkyl groups directly bonded to the chal

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