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Benzene, 1-ethenyl-4-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16262-48-9

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16262-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16262-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16262-48:
(7*1)+(6*6)+(5*2)+(4*6)+(3*2)+(2*4)+(1*8)=99
99 % 10 = 9
So 16262-48-9 is a valid CAS Registry Number.

16262-48-9Downstream Products

16262-48-9Relevant academic research and scientific papers

Visible-Light-Induced Meerwein Fluoroarylation of Styrenes

Tang, Hai-Jun,Zhang, Bin,Xue, Fei,Feng, Chao

supporting information, p. 4040 - 4044 (2021/05/26)

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.

Formal Allylation and Enantioselective Cyclopropanation of Donor/Acceptor Rhodium(II) Azavinyl Carbenes

Liu, Zhili,Chen, Lianfen,Zhu, Dong,Zhu, Shifa

, p. 1275 - 1279 (2021/02/20)

A highly efficient formal allylation of dihydronaphthotriazoles with alkenes under rhodium(II) catalysis is reported. Various allyl dihydronaphthalene derivatives were furnished via rhodium(II) azavinyl carbenes with moderate to good yields and excellent chemoselectivity. When monosubstituted alkenes are used, cyclopropanation occurs and good to excellent enantioselectivities have been achieved. Particularly noteworthy is the allylic C(sp2)-H activation instead of traditional C(sp3)-H activation in the formal allylation process.

Living anionic polymerization of 4-(α-alkylvinyl)styrene derivatives

Hirao, Akira,Imai, Takahiro,Watanabe, Kenji,Hayashi, Mayumi,Sugiyama, Kenji

, p. 855 - 867 (2007/10/03)

The anionic polymerization of four bis-functionalized styrene derivatives with α-alkylvinyl groups have been carried out in THF at -78°C with the initiator prepared from oligo(α-methylstyryl)lithium and potassium tert-butoxide. The four monomers herein us

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