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2-Propenenitrile, 2-[(acetyloxy)methyl]-3-phenyl-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

177838-08-3

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177838-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 177838-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,8,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 177838-08:
(8*1)+(7*7)+(6*7)+(5*8)+(4*3)+(3*8)+(2*0)+(1*8)=183
183 % 10 = 3
So 177838-08-3 is a valid CAS Registry Number.

177838-08-3Relevant academic research and scientific papers

Montmorillonite K10 clay-microwave assisted isomerisation of acetates of the Baylis-Hillman adducts: A facile method of stereoselective synthesis of (e)-trisubstituted alkenes

Shanmugam,Singh

, p. 1314 - 1316 (2001)

Montmorillonite K10-microwave assisted stereoselective isomerisation of acetates of the Baylis-Hillman adducts furnished (E)-trisubstituted alkenes in high yields. A comparative study of this reaction with Mont-K10, ion-exchanged clay (Fe3+-Mont-K10) and acid treated regional natural Kaolinite clay and the efficiency of these clays in this reaction is described.

Palladium-catalyzed arylation of methyl 2-(acetoxymethyl)acrylate: A convenient synthesis of rearranged Morita-Baylis-Hillman acetates

Kim, Ko Hoon,Lim, Jin Woo,Lee, Hyun Ju,Kim, Jae Nyoung

, p. 419 - 423 (2013/02/25)

Palladium-catalyzed arylation of methyl 2-(acetoxymethyl)acrylate with aryl iodides afforded the primary acetates of Morita-Baylis-Hillman adducts in good yields with high stereoselectivity under mild conditions (50°C).

Bismuth triflate-catalyzed rearrangement of acetates of the Baylis-Hillman adducts into (E)-trisubstituted alkenes

Ollevier, Thierry,Mwene-Mbeja, Topwe M.

, p. 5150 - 5155 (2008/09/21)

In the presence of a catalytic amount of bismuth triflate, methyl 3-acetoxy-3-aryl-2-methylenepropanoates and 3-acetoxy-3-aryl-2-methylenepropanitriles were smoothly converted into methyl (2E)-2-(acetoxymethyl)-3-arylprop-2-enoates and (2E)-2-(acetoxymeth

Studies on montmorillonite K10-microwave assisted isomerisation of Baylis-Hillman adduct. Synthesis of E-trisubstituted alkenes and synthetic application to lignan core structures by vinyl radical cyclization

Shanmugam, Ponnusamy,Rajasingh, Paramasivan

, p. 9283 - 9295 (2007/10/03)

The isomerisation of acetates from the Baylis-Hillman adducts with Mont.K10 clay-microwave combination furnished E-trisubstituted alkenes in high yield. The simple Baylis-Hillman adducts with trimethyl orthoformate and unsaturated alcohols under clay cata

TMSOTf-catalyzed stereoselective isomerization of acetates of the Baylis-Hillman adducts

Basavaiah, Deevi,Muthukumaran, Kannan,Sreenivasulu, Bandaru

, p. 545 - 548 (2007/10/03)

TMSOTf-catalyzed isomerization of acetates of the Baylis-Hillman adducts, i.e. methyl 3-acetoxy-3-aryl-2-methylenepropanoates and 3-acetoxy-3- aryl-2-methylenepropanenitriles pro-viding methyl (2E)-2-(acetoxymethyl)-3- arylprop-2-enoates and (2E)-2-(aceto

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