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38226-17-4

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38226-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38226-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38226-17:
(7*3)+(6*8)+(5*2)+(4*2)+(3*6)+(2*1)+(1*7)=114
114 % 10 = 4
So 38226-17-4 is a valid CAS Registry Number.

38226-17-4Relevant articles and documents

Fluoroalkylselenolation of Alkyl Silanes/Trifluoroborates under Metal-Free Visible-Light Photoredox Catalysis

Ghiazza, Clément,Khrouz, Lhoussain,Billard, Thierry,Monnereau, Cyrille,Tlili, Anis

supporting information, p. 1559 - 1566 (2019/11/03)

Herein a metal-free fluoroalkylselenolation of alkylsilanes as well as potassium alkyltrifluoroborates under visible light photocatalysis is disclosed. The developed methodologies are performed under mild conditions, room temperature in the presence of an organic photocatalyst and blue LED irradiation. Mechanistic investigations including luminescence and EPR spectroscopy allow us to shed light on both mechanisms.

Stereoselective peterson olefinations from bench-stable reagents and N-phenyl imines

Das, Manas,Manvar, Atul,Jacolot, Ma?wenn,Blangetti, Marco,Jones, Roderick C.,O'Shea, Donal F.

supporting information, p. 8737 - 8740 (2015/06/08)

The synthesis of bench-stable α,α-bis(trimethylsilyl)toluenes and tris(trimethylsilyl)methane is described and their use in stereoselective Peterson olefinations has been achieved with a wide substrate scope. Product stereoselectivity was poor with carbonyl electrophiles (E/Z ~1:1 to 4:1) though this was significantly improved by employing the corresponding substituted N-benzylideneaniline (up to 99:1) as an alternative electrophile. The olefination byproduct was identified as N,N-bis(trimethylsilyl)aniline and could be easily separated from product by aqueous acid extraction. Evidence for an autocatalytic cycle has been obtained.

Synthesis of α-Lithioarylmethanes of m-Xylene and its α-Trimethylsilyl Derivatives; Crystal Structure of 2>

Engelhardt, Lutz M.,Leung, Wing-Por,Raston, Colin L.,White, Allan H.

, p. 337 - 344 (2007/10/02)

Crystalline organolithium complexes > (R=R'=H, R=R'=SiMe3, pmdien=NNN'N"N"-pentamethyldiethylenetriamine), > (tmen=NNN'N'-tetramethylethylenediamine), and 2> have

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