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1351520-69-8

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1351520-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1351520-69-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,1,5,2 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1351520-69:
(9*1)+(8*3)+(7*5)+(6*1)+(5*5)+(4*2)+(3*0)+(2*6)+(1*9)=128
128 % 10 = 8
So 1351520-69-8 is a valid CAS Registry Number.

1351520-69-8Downstream Products

1351520-69-8Relevant articles and documents

Regiodivergent hydrosilylation, hydrogenation, [2π + 2π]-cycloaddition and C-H borylation using counterion activated earth-abundant metal catalysis

Agahi, Riaz,Challinor, Amy J.,Dunne, Joanne,Docherty, Jamie H.,Carter, Neil B.,Thomas, Stephen P.

, p. 5079 - 5084 (2019)

The widespread adoption of earth-abundant metal catalysis lags behind that of the second- and third-row transition metals due to the often challenging practical requirements needed to generate the active low oxidation-state catalysts. Here we report the development of a single endogenous activation protocol across five reaction classes using both iron- and cobalt pre-catalysts. This simple catalytic manifold uses commercially available, bench-stable iron- or cobalt tetrafluoroborate salts to perform regiodivergent alkene and alkyne hydrosilylation, 1,3-diene hydrosilylation, hydrogenation, [2π + 2π]-cycloaddition and C-H borylation. The activation protocol proceeds by fluoride dissociation from the counterion, in situ formation of a hydridic activator and generation of a low oxidation-state catalyst.

Nickel-Catalyzed Hydrosilylation of Terminal Alkenes with Primary Silanes via Electrophilic Silicon-Hydrogen Bond Activation

Wu, Xiaoyu,Ding, Guangni,Lu, Wenkui,Yang, Liqun,Wang, Jingyang,Zhang, Yuxuan,Xie, Xiaomin,Zhang, Zhaoguo

supporting information, p. 1434 - 1439 (2021/02/16)

We report a simple and effective nickel-based catalytic system, NiCl2·6H2O/tBuOK, for the electrophilically activated hydrosilylation of terminal alkenes with primary silanes. This protocol provides excellent performance under mild reaction conditions: ex

Manganese-Catalyzed Hydrofunctionalization of Alkenes

Carney, Jonathan R.,Dillon, Barry R.,Campbell, Leonie,Thomas, Stephen P.

supporting information, p. 10620 - 10624 (2018/07/31)

The manganese-catalyzed hydrosilylation and hydroboration of alkenes has been developed using a single manganese(II) precatalyst and reaction protocol. Both reactions proceed with excellent control of regioselectivity and in high yields across a variety of sterically and electronically differentiated substrates (25 examples). Alkoxide activation, using NaOtBu, was key to precatalyst activation and reactivity. Catalysis was achieved across various functional groups and on gram-scale for both the developed methodologies with catalysts loadings as low as 0.5 mol %.

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