Welcome to LookChem.com Sign In|Join Free
  • or
2-Propenoic acid, 3-(phenyltelluro)-, ethyl ester, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82296-85-3

Post Buying Request

82296-85-3 Suppliers

Recommended suppliers

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

82296-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82296-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82296-85:
(7*8)+(6*2)+(5*2)+(4*9)+(3*6)+(2*8)+(1*5)=153
153 % 10 = 3
So 82296-85-3 is a valid CAS Registry Number.

82296-85-3Relevant academic research and scientific papers

Organylzinc chalcogenolate promoted michael-type addition of α,β-unsaturated carbonyl compounds

Loren Nunes, Vanessa,De Oliveira, Ingryd Cristina,Soares Do Rego Barros, Olga

supporting information, p. 1525 - 1530 (2014/03/21)

We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage of diorganyl dichalcogenide bonds by the Zn/NH 4OH system led to organylz

Organylzinc Chalcogenolate Promoted Michael-Type Addition of α,β-Unsaturated Carbonyl Compounds

L?ren Nunes, Vanessa,De Oliveira, Ingryd Cristina,Soares Do Rêgo Barros, Olga

supporting information, p. 1525 - 1530 (2015/10/05)

We present the chemo-, regio-, and stereoselective synthesis of vinyl chalcogenide compounds promoted by organylzinc chalcogenolates. In this protocol, reductive cleavage of diorganyl dichalcogenide bonds by the Zn/NH4OH system led to organylzi

PHOSPHINE-NICKEL(II), -COBALT(II), -PALLADIUM(0) AND -PALLADIUM(II) COMPLEXES AS CATALYSTS IN CROSS-COUPLING REACTIONS OF ARYL- AND ALKYL-GRIGNARD REAGENTS WITH ORGANIC TELLURIDES

Uemura, Sakae,Fukuzawa, Shin-Ichi,Patil, Suresh R.

, p. 9 - 18 (2007/10/02)

Some alkyl- and aryl-tellurides react with Grignard reagents (RMgBr; R = aryl and alkyl) in the presence of NiCl2(PPh3)2, NiCl2(Ph2PCH2CH2CH2PPh2), or CoCl2(PPh3)2 as catalyst in THF or diethyl ether as solvent to give the cross-coupling products together with the homo-coupling products of the tellurides in good to moderate yields, with elemental tellurium being formed as a black precipitate.A catalytic reduction-oxidation cycle involving a Ni or Co complex bearing an organotellurium moiety (RTe; R = alkenyl, aryl, and alkyl) is proposed for the reaction.Palladium catalysts such as Pd(PPh3)4, PdCl2(PPh3)2, and PdCl2(PhCN)2 are revealed to be much less effective than the Ni and Co catalysts in both the yield and the stereoselectivity of the product.

Ni(II)- AND Co(II)-PHOSPHINE COMPLEX CATALYZED CARBON-CARBON BOND FORMATION BETWEEN ORGANIC TELLURIDES AND GRIGNARD REAGENTS

Uemura, Sakae,Fukuzawa, Shin-ichi

, p. 1181 - 1184 (2007/10/02)

Treatment of alkenyl and aryl tellurides with Grignard reagents in the presence of NiCl2(PPh3)2, NiCl2(Ph2PCH2CH2CH2PPh2), or CoCl2(PPh3)2 as catalyst affords the cross-coupling products together with the homo-coupling products of the tellurides in good to moderate yields under mild conditions.

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 82296-85-3