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Silane, (1,1-dimethylethyl)[(3Z)-3-pentenyloxy]diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

494796-91-7

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494796-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494796-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,7,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 494796-91:
(8*4)+(7*9)+(6*4)+(5*7)+(4*9)+(3*6)+(2*9)+(1*1)=227
227 % 10 = 7
So 494796-91-7 is a valid CAS Registry Number.

494796-91-7Relevant academic research and scientific papers

Toward amide-linked RNA mimics: Total synthesis of 3′-C branched uridine azido acid via an ene-iodolactonization approach

Rozners, Eriks,Liu, Yang

, p. 181 - 184 (2003)

(Matrix presented) A novel synthesis of 3′-C branched uridine azido acid has been accomplished by a sequence of stereoselective ene and iodolactonization reactions. Compared to traditional routes that start from carbohydrates, the present methodology is m

Migratory Hydrogenation of Terminal Alkynes by Base/Cobalt Relay Catalysis

Liu, Bingxue,Liu, Qiang,Liu, Xufang

, p. 6750 - 6755 (2020/03/13)

Migratory functionalization of alkenes has emerged as a powerful strategy to achieve functionalization at a distal position to the original reactive site on a hydrocarbon chain. However, an analogous protocol for alkyne substrates is yet to be developed. Herein, a base and cobalt relay catalytic process for the selective synthesis of (Z)-2-alkenes and conjugated E alkenes by migratory hydrogenation of terminal alkynes is disclosed. Mechanistic studies support a relay catalytic process involving a sequential base-catalyzed isomerization of terminal alkynes and cobalt-catalyzed hydrogenation of either 2-alkynes or conjugated diene intermediates. Notably, this practical non-noble metal catalytic system enables efficient control of the chemo-, regio-, and stereoselectivity of this transformation.

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