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1-(4-methoxyphenyl)ethane-1,2-diyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86659-43-0

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86659-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86659-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86659-43:
(7*8)+(6*6)+(5*6)+(4*5)+(3*9)+(2*4)+(1*3)=180
180 % 10 = 0
So 86659-43-0 is a valid CAS Registry Number.

86659-43-0Relevant academic research and scientific papers

Visible light induced redox neutral fragmentation of 1,2-diol derivatives

Chen, Kang,Schwarz, Johanna,Karl, Tobias A.,Chatterjee, Anamitra,K?nig, Burkhard

, p. 13144 - 13147 (2019/11/11)

A homogeneous, redox-neutral photo fragmentation of diol derivatives was developed. Under photo/hydrogen atom transfer (HAT) dual catalysis, diol derivatives such as lignin model compounds and diol monoesters undergo selective β C(sp3)-O bond cleavage to afford ketones, phenols and acids effectively.

B2pin2-Mediated Palladium-Catalyzed Diacetoxylation of Aryl Alkenes with O2 as Oxygen Source and Sole Oxidant

Huang, Jiuzhong,Ouyang, Lu,Li, Jianxiao,Zheng, Jia,Yan, Wuxin,Wu, Wanqing,Jiang, Huanfeng

supporting information, p. 5090 - 5093 (2018/09/12)

A novel palladium-catalyzed alkene diacetoxylation with dioxygen (O2) as both the sole oxidant and oxygen source is developed, which was identified by 18O-isotope labeling studies. Control experiments suggested that bis(pinacolato)diboron (B2pin2) played a dominant intermediary role in the formation of a C-O bond. This method performed good functional group tolerance with moderate to excellent yields, which could be successfully applied to the late-stage modification of natural products. Furthermore, an atmospheric pressure of dioxygen enhances the practicability of the protocol.

Vicinal Difunctionalization of Alkenes under Iodine(III) Catalysis involving Lewis Base Adducts

Aertker, Kristina,Rama, Raquel J.,Opalach, Julita,Mu?iz, Kilian

, p. 1290 - 1294 (2017/04/18)

The influence of a 2-pyridinyl substituent on the catalytic performance of aryl iodides as catalyst in iodine(III) chemistry was explored. An efficient Lewis base adduct between the pyridine nitrogen and the electrophilic iodine(III) center was identified and confirmed by X-ray analysis. This arrangement was shown to generate a kinetically competent superior catalyst structure for the catalytic dioxygenation of alkenes. It introduces the concept of Lewis base adduct formation as a kinetic factor in iodine(I/III) catalysis. (Figure presented.).

Bis(NHC)-palladium(II) complex-catalyzed dioxygenation of alkenes

Wang, Wenfeng,Wang, Feijun,Shi, Min

experimental part, p. 928 - 933 (2010/05/01)

Bis(NHC)-Pd(II) complexes derived from l,l'-binaphthyl-2,2'-diamine (BINAM) were successfully first used to catalyze the dioxygenation of alkenes under mild conditions tolerant of air and moisture. Cationic NHC-Pd2+ diaquo complex 1e showed the highest catalytic activity to give 1,2dioxygenation products with good syn-diastereoselectivity for 1,2-disubstituted alkenes.

Electron-transfer Processes: Oxidation of α- and β-Alkenylbenzenes by Peroxydisulphate in Acetic Acid

Citterio, Attilio,Arnoldi, Claudio,Giordano, Claudio,Castaldi, Grasiano

, p. 891 - 896 (2007/10/02)

Oxidation of α- and β-unsaturated alkylbenzenes by peroxydisulphate in acetic acid gives side-chain acetoxylation with formation of the corresponding glycol diacetates and compounds (10), respectively.The reaction is catalysed by transition-metal salts, among which cupric acetate gives the best results.Generally, electron-releasing substituents on the benzene ring increase the yield and improve the selectivity.The same substrates are oxidized in water under Ag+ catalysis to the corresponding aldehydes.The different behaviour in the two solvents is ascribed to the difference in reactivity between the primary oxidation products and the starting olefin, whereas the initial oxidation step is suggested to occur in both cases via an electron-transfer process from the olefin to the sulphate radical anion.

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