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Butanoic acid, 4-(2-iodophenoxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132902-23-9

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132902-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132902-23-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,0 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132902-23:
(8*1)+(7*3)+(6*2)+(5*9)+(4*0)+(3*2)+(2*2)+(1*3)=99
99 % 10 = 9
So 132902-23-9 is a valid CAS Registry Number.

132902-23-9Relevant academic research and scientific papers

Alkylation-Terminated Catellani Reactions Using Alkyl Carbagermatranes

Jiang, Wei-Tao,Xiao, Bin,Xie, Xiu-Ying,Xu, Meng-Yu,Yang, Shuo

supporting information, p. 20450 - 20454 (2020/09/07)

The Catellani reaction has received substantial attention because it enables rapid multiple derivatization on aromatics. While using alkyl electrophiles to achieve ortho-alkylation was one of the earliest applications of the Catellani reaction, ipso-alkyl

Synthesis and biological evaluation of new quinoxaline derivatives of ICF01012 as melanoma-targeting probes

El Aissi, Radhia,Liu, Jianrong,Besse, Sophie,Canitrot, Damien,Chavignon, Olivier,Chezal, Jean-Michel,Miot-Noirault, Elisabeth,Moreau, Emmanuel

supporting information, p. 468 - 473 (2014/06/09)

The aim of this study was the synthesis and pharmacokinetic selection of a best melanin-targeting ligand for addressing anticancer agents to pigmented melanoma. Seven quinoxaline carboxamide derivatives were synthesized and radiolabeled with iodine-125. Biodistribution studies of compounds [ 125I]1a-g performed in melanoma-bearing mice tumor showed significant tumor uptake (range 2.43-5.68%ID/g) within 1 h after i.v. injection. Fast clearance of the radioactivity from the nontarget organs mainly via the urinary system gave high tumor-to-blood and tumor-to-muscle ratios. Given its favorable clearance and high tumor-melanoma uptake at 72 h, amide 1d was the most promising melanoma-targeting ligand in this series. Compound 1d will be used as building block for the design of new melanoma-selective drug delivery systems.

Development of new recyclable reagents and catalytic systems based on hypervalent iodine compounds

Yusubov, Mekhman S.,Zhdankin, Viktor V.

scheme or table, p. 185 - 191 (2011/03/19)

Recent advances in the development of polymer-supported iodine(V) oxidants, recyclable monomeric hypervalent iodine(III) reagents and catalytic systems based on hypervalent iodine compounds are discussed. These efficient and environmentally friendly reagents and catalysts are particularly useful for oxidative transformations of alcohols to carbonyl compounds and for oxidations at the benzylic position.

Preparation and reactivity of polymer-supported 2-iodylphenol ethers, an efficient recyclable oxidizing system

Karimov, Rashad R.,Kazhkenov, Zeinul-Gabiden M.,Modjewski, Matthew J.,Peterson, Eric M.,Zhdankin, Viktor V.

, p. 8149 - 8151 (2008/02/13)

(Chemical Equation Presented) Preparation of new recyclable polymer-supported oxidizing reagents based on 2-iodylphenol ethers is described. The synthesis employs commercially available aminomethylated polystyrene or Merrifield resin and affords polymer-supported 2-iodylphenol ethers with loading up to 0.86 mmol/g with respect to IO2 groups. The new reagents effect clean and efficient conversion of a wide range of alcohols, including heteroatomic and unsaturated structures, to the corresponding carbonyl compounds. Recycling of the resins is possible with minimal loss of activity after several reoxidations.

The First Direct Chlorination of Iodoarenes - A Side-chain Directed Process

Mirk, Daniela,Kataeva, Olga,Froehlich, Roland,Waldvogel, Siegfried R.

, p. 2410 - 2414 (2007/10/03)

The chlorination of electron rich iodoarenes with MoCl5 proceeds with methoxycarbonylmethyl as the directing group. The transformation is selective and without loss of the valuable iodo substituent.

Leukotriene-B4 derivatives, process for their production and their use as pharmaceutical agents

-

, (2008/06/13)

The invention relates to leukotriene-B4 derivatives of formula I, STR1 in which n=1-10, R1 means radical CH2 OH, radical COOR4, radical CONHR5 or radical CONR6 R7, A means a cis,

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