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[2-benzyl-1-(4-methoxy-phenyl)-allyloxy]-triethyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

930806-58-9

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930806-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 930806-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,0,8,0 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 930806-58:
(8*9)+(7*3)+(6*0)+(5*8)+(4*0)+(3*6)+(2*5)+(1*8)=169
169 % 10 = 9
So 930806-58-9 is a valid CAS Registry Number.

930806-58-9Relevant academic research and scientific papers

Bench-Stable N-Heterocyclic Carbene Nickel Precatalysts for C?C and C?N Bond-Forming Reactions

Strieth-Kalthoff, Felix,Longstreet, Ashley R.,Weber, Jessica M.,Jamison, Timothy F.

, p. 2873 - 2877 (2018/05/07)

Herein, we introduce a new class of bench-stable N-heterocyclic carbene (NHC) nickel-precatalysts for homogeneous nickel-catalysis. The nickel(II) complexes are readily activated to Ni0 in situ under mild conditions, via a proposed Heck-type me

Nitrile assisted, Bronsted acid catalyzed regio and stereoselective diarylphosphonylation of allyl silyl ethers

Ho, Chun-Yu,Chan, Chun-Wa,Wo, Siu-Kwan,Zuo, Zhong,Chan, Lai-Ying

supporting information; experimental part, p. 3480 - 3487 (2010/08/21)

We have discovered a mild, catalytic protocol for the regio- and stereoselective synthesis of trisubstituted allyl diarylphosphonates from the corresponding disubstituted allyl silyl ethers, circumventing the challenges related to the preparation and availability of stereodefined trisubstituted olefins. A closely related arylation reaction was also discovered during the methodology development. By simply switching the reaction medium, high phosphonylation/arylation ratios and vice versa can be achieved. This may not be a direct result of changing solvent polarity. The allyl diarylphosphonates were evaluated as carboxylesterase inhibitors, and the screening results revealed that the inhibitory efficiency is highly related to the choice of alkenes and aryl substituents. The Royal Society of Chemistry 2010.

Highly selective coupling of alkenes and aldehydes catalyzed by [Ni(NHC){P(OPh)3}]: Synergy between a strong σ donor and a strong π acceptor

Ho, Chun-Yu,Jamison, Timothy F.

, p. 782 - 785 (2007/10/03)

(Chemical Equation Presented) Give and take: Both a strong electron donor (1) and a strong electron acceptor (P(OPh)3) are necessary for a highly selective, nickel-catalyzed coupling reaction between alkenes, aldehydes, and silyl triflates (see

Nickel-catalyzed coupling of alkenes, aldehydes, and silyl triflates

Ng, Sze-Sze,Ho, Chun-Yu,Jamison, Timothy F.

, p. 11513 - 11528 (2007/10/03)

A full account of two recently developed nickel-catalyzed coupling reactions of alkenes, aldehydes, and silyl triflates is presented. These reactions provide either allylic alcohol or homoallylic alcohol derivatives selectively, depending on the ligand em

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