Welcome to LookChem.com Sign In|Join Free
  • or
diethyl (E)-(4-phenylbut-1-en-1-yl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135760-96-2

Post Buying Request

135760-96-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

135760-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135760-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,7,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 135760-96:
(8*1)+(7*3)+(6*5)+(5*7)+(4*6)+(3*0)+(2*9)+(1*6)=142
142 % 10 = 2
So 135760-96-2 is a valid CAS Registry Number.

135760-96-2Relevant academic research and scientific papers

Remote Functionalization of α,β-Unsaturated Carbonyls by Multimetallic Sequential Catalysis

Romano, Ciro,Fiorito, Daniele,Mazet, Clément

, p. 16983 - 16990 (2019)

The remote functionalization of α,β-unsaturated carbonyls by an array of multimetallic sequential catalytic systems is described. The reactions are triggered by hydrometalation using [Pd-H] or [Ru-H] isomerization catalysts and driven by the formation of thermodynamically more stable 1,2-vinyl arenes. The Pd-catalyzed deconjugative isomerization was combined with a Cu-catalyzed β-borylation of the transiently generated styrenyl derivatives to deliver a range of products that would not be accessible with the use of a single catalyst. [Pd/Cu] catalytic systems were also identified for the highly enantioselective α-hydroboration and α-hydroamination of the styrenyl intermediates. Difunctionalization simultaneously at the benzylic and homobenzylic positions was achieved by combining the isomerization process with Sharpless asymmetric dihydroxylation (SAD) using [Pd/Os] or [Ru/Os] couples. Starting from a simple α,β-unsaturated ester, an isomerization/dihydroxylation/lactonization sequence gave access to a naturally occurring γ-butyrolactone in good yield, with excellent diastereo- and enantioselectivity.

Phosphonate vs. phosphinate elimination during olefination of aldehydes

Prashad, Mahavir

, p. 1585 - 1588 (1993)

Olefination of aldehydes with O,O,O-triethyl methylmethylenephosphonophosphinate in the presence of magnesium bromide etherate and triethylamine leads to a selective elimination of the phosphonate group over the phosphinate to yield alkenyl(methyl)phosphi

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 135760-96-2