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((3-iodoprop-2-yn-1-yl)oxy)benzene is an organic compound characterized by its unique structure, which features a benzene ring with an iodine atom attached to a propargyl group. The propargyl group consists of a three-carbon chain with a triple bond between the first and second carbons, and an oxygen atom connected to the third carbon. This oxygen atom is further bonded to the benzene ring, creating an ether linkage. The presence of the iodine atom in this molecule makes it a potentially valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as in materials science for the development of new compounds with specific properties. The compound's reactivity and the ability to form various derivatives make it an interesting subject for chemical research and development.

1725-81-1

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1725-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1725-81-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1725-81:
(6*1)+(5*7)+(4*2)+(3*5)+(2*8)+(1*1)=81
81 % 10 = 1
So 1725-81-1 is a valid CAS Registry Number.

1725-81-1Relevant 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 1,2,3-triazole-fused heterocycles via Pd-catalyzed cyclization of 5-iodotriazoles

Schulman, Jacqueline M.,Friedman, Adam A.,Panteleev, Jane,Lautens, Mark

, p. 55 - 57 (2012/01/05)

A convenient approach toward polycyclic frameworks containing fused 1,2,3-triazoles is described. The synthesis consists of a Cu-catalyzed cycloaddition and an intramolecular Pd-catalyzed direct arylation or Heck reaction, and affords the products in good to excellent yields.

Design, synthesis and biological evaluation of novel 2-methylpyrimidine-4- ylamine derivatives as inhibitors of Escherichia coli pyruvate dehydrogenase complex E1

He, Junbo,Feng, Lingling,Li, Jing,Tao, Ruijuan,Wang, Fang,Liao, Xun,Sun, Qiushuang,Long, Qingwu,Ren, Yanliang,Wan, Jian,He, Hongwu

, p. 1665 - 1670 (2012/04/10)

As potential inhibitors of Escherichia coli pyruvate dehydrogenase complex E1 (PDHc E1), a series of novel 2-methylpyrimidine-4-ylamine derivatives were designed based on the structure of the active site of PDHc E1 and synthesized using 'click chemistry'.

Influence of the acetylenic substituent on the intramolecular carbolithiation of alkynes

Girard, Anne-Lise,Lhermet, Rudy,Fressigne, Catherine,Durandetti, Muriel,Maddaluno, Jacques

experimental part, p. 2895 - 2905 (2012/06/29)

The intramolecular carbolithiation of a series of propargylic ethers has been performed to evaluate the influence of the terminal substituent on the efficiency and the stereochemical outcome of the cyclization. Our results show that only 5-exo-dig cyclizations are observed, and dihydrobenzofurans are obtained exclusively. Depending on the nature of the terminal substituent, two cases can be considered. If the terminal substituent carried by the acetylenic carbon atom is itself a carbon atom, the cyclization can occur provided the terminal propargylic position bears a coordinating element and is at least disubstituted. When the cyclization occurs, it follows an anti-carbolithiation pathway and thus leads to the E isomer of the exocyclic double bond. Only in one case (Ph) was a mixture of the E and Z isomers of the resulting olefin recovered. The cyclization can also take place if the alkyne is directly substituted by S or Si, provided the cyclization conditions are tuned. In the case of the trimethylsilyl substituent, a syn-carbolithiation was observed. If the double bond is recovered, in most cases, in the exocyclic position, the products can aromatize directly for SPh-substituted substrate 24. Furthermore, in the two latter cases, when alkylation of the vinyllithium intermediate is performed, isomerization of the double bond seems instantaneous. Copyright

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