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(5RS,6SR)-5-iodo-6-phenyltetrahydro-2H-pyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100238-90-2

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100238-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100238-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,3 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100238-90:
(8*1)+(7*0)+(6*0)+(5*2)+(4*3)+(3*8)+(2*9)+(1*0)=72
72 % 10 = 2
So 100238-90-2 is a valid CAS Registry Number.

100238-90-2Downstream Products

100238-90-2Relevant academic research and scientific papers

Lewis base catalysis of bromo- and iodolactonization, and cycloetherification

Denmark, Scott E.,Burk, Matthew T.

, p. 20655 - 20660 (2010)

Lewis base catalyzed bromo- and iodolactonization reactions have been developed and the effects of catalyst structure on rate and cyclization selectivity have been systematically explored. The effects of substrate structure on halolactonization reactions

trans-Cyclooctenes as Halolactonization Catalysts

Einaru, Shunsuke,Shitamichi, Kenta,Nagano, Tagui,Matsumoto, Akira,Asano, Keisuke,Matsubara, Seijiro

, p. 13863 - 13867 (2018/09/27)

The strained olefins in trans-cyclooctenes serve as efficient catalysts for halolactonizations, including bromolactonizations and iodolactonizations. The trans-cyclooctene framework is essential for excellent catalytic performance, and the substituents also play important roles in determining efficiency. These results are the first demonstration of catalysis by a trans-cyclooctene.

A Formal Intermolecular Iodolactonization Reaction Based on a Radical-Ionic Sequence

León-Rayo, David F.,Morales-Chamorro, Maricela,Cordero-Vargas, Alejandro

, p. 1739 - 1750 (2016/04/05)

We report herein a method based on a radical-ionic sequence between an allylic alcohol and an α-iodo acid in the presence of substoichiometric amounts of lauroyl peroxide (DLP) to produce an atom transfer radical addition (ATRA) adduct, which subseqently

4-(Dimethylamino)pyridine-catalysed iodolactonisation of γ,δ-unsaturated carboxylic acids

Meng, Chuisong,Liu, Zhihui,Liu, Yuxiu,Wang, Qingmin

supporting information, p. 6766 - 6772 (2015/06/25)

4-(Dimethylamino)pyridine functioned as an excellent catalyst for iodolactonisation reactions of γ,δ-unsaturated carboxylic acids, affording γ-lactones, δ-lactones, or both under neutral conditions at room temperature. The effects of substrate structures

LEAD(IV) ACETATE-METAL HALIDE REAGENTS III. A NEW METHOD FOR THE SYNTHESIS OF TETRAHYDROFURAN, TETRAHYDROPYRAN AND LACTONE DERIVATIVES

Motohashi, Shigeyasu,Satomi, Masakichi,Fujimoto, Yasuo,Tatsuno, Takashi

, p. 2035 - 2039 (2007/10/02)

A new method for the synthesis of tetrahydrofuran, tetrahydropyran and lactone derivatives from γδ-, δε-unsaturated alcohols and βγ-, γδ-carboxylic acids is described.

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