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2-<2-(4'-Methoxyphenyl)-ethyl>-acrylsaeureethylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77831-87-9

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77831-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77831-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77831-87:
(7*7)+(6*7)+(5*8)+(4*3)+(3*1)+(2*8)+(1*7)=169
169 % 10 = 9
So 77831-87-9 is a valid CAS Registry Number.

77831-87-9Relevant academic research and scientific papers

Alkylation of Allyl/Alkenyl Sulfones by Deoxygenation of Alkoxyl Radicals

Han, Jia-Bin,Guo, Ao,Tang, Xiang-Ying

supporting information, p. 2989 - 2994 (2019/02/05)

A challenging deoxygenation of alkoxyl radicals from readily accessible alcohol derivatives was developed, affording facile synthesis of functionalized alkenes with good functional group tolerance under mild reaction conditions. Because alkoxyl radicals can easily undergo β-fragmentations or hydrogen abstractions, this new strategy for deoxygenation of alkoxyl radicals is highly valuable. Moreover, mechanistic studies revealed that the electron-neutral phosphine acts as the deoxygenation reagent.

Donor–Acceptor Complex Enables Alkoxyl Radical Generation for Metal-Free C(sp3)–C(sp3) Cleavage and Allylation/Alkenylation

Zhang, Jing,Li, Yang,Xu, Ruoyu,Chen, Yiyun

, p. 12619 - 12623 (2017/09/11)

The alkoxyl radical is an essential and prevalent reactive intermediate for chemical and biological studies. Here we report the first donor–acceptor complex-enabled alkoxyl radical generation under metal-free reaction conditions induced by visible light. Hantzsch ester forms the key donor–acceptor complex with N-alkoxyl derivatives, which is elucidated by a series of spectrometry and mechanistic experiments. Selective C(sp3)-C(sp3) bond cleavage and allylation/alkenylation is demonstrated for the first time using this photocatalyst-free approach with linear primary, secondary, and tertiary alkoxyl radicals.

Phosphinic acid-based MMP-13 inhibitors that spare MMP-1 and MMP-3

Reiter, Lawrence A.,Mitchell, Peter G.,Martinelli, Gary J.,Lopresti-Morrow, Lori L.,Yocum, Sue A.,Eskra, James D.

, p. 2331 - 2336 (2007/10/03)

Phosphinic acid-based inhibitors of MMP-13 have been investigated with the aim of identifying potent inhibitors with high selectivity versus MMP-1. Independent variation of the substituents on a P1′ phenethyl group and a P2 benzyl gr

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