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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.

92287-20-2

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92287-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92287-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,8 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92287-20:
(7*9)+(6*2)+(5*2)+(4*8)+(3*7)+(2*2)+(1*0)=142
142 % 10 = 2
So 92287-20-2 is a valid CAS Registry Number.

92287-20-2Downstream Products

92287-20-2Relevant academic research and scientific papers

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

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

, p. 6766 - 6772 (2015)

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

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

Lewis base catalysis of bromo- and iodolactonization, and cycloetherification

Denmark, Scott E.,Burk, Matthew T.

experimental part, p. 20655 - 20660 (2011/10/12)

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

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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