Welcome to LookChem.com Sign In|Join Free
  • or
1-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80859-83-2

Post Buying Request

80859-83-2 Suppliers

Recommended suppliers

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

80859-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80859-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,5 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80859-83:
(7*8)+(6*0)+(5*8)+(4*5)+(3*9)+(2*8)+(1*3)=162
162 % 10 = 2
So 80859-83-2 is a valid CAS Registry Number.

80859-83-2Relevant academic research and scientific papers

A benzene-bridged divanadium complex-early transition metal catalyst for alkene alkylarylation with PhI(O2CR)2viadecarboxylation

Zhang, Lei,Zhou, Hongfei,Bai, Shaokun,Li, Shaodan

supporting information, p. 3201 - 3206 (2021/03/16)

The synthesis, structure and catalytic activity of a benzene-bridged divanadium complex were comprehensively studied. The reduction of (Nacnac)VCl2(1) (Nacnac = (2,6-iPr2C6H3NCMe)2HC) supported by β-diketiminate with potassium graphite (KC8) by employing benzene as the solvent allows access to the benzene-bridged inverted-sandwich divanadium complex (μ-η6:η6-C6H6)[V(Nacnac)]2(2a), which can catalyze alkene alkylarylation with hypervalent iodine(iii) reagents (HIRs)viadecarboxylation to generate regioselectively diverse indolinones. Furthermore, the mild nature of this reaction was amenable to a wide range of functionalities on alkenes and HIRs. Mechanistic studies revealed a relay sequence of decarboxylative radical alkylation/radical arylation/oxidative re-aromatization.

Peptidomimetic synthesis by way of diastereoselective iodoacetoxylation and transannular amidation of 7-9-membered lactams

Atmuri, N.D. Prasad,Reilley, David J.,Lubell, William D.

supporting information, p. 5066 - 5069 (2017/11/07)

Azacyclo-and azabicycloalkanone peptidomimetics were synthesized regio-and diastereoselectively by iodoacetoxylation and transannular amidation reactions on unsaturated lactam precursors contingent on ring size olefin position solvent and hypervalent iodi

Reactivity of arenes in substitution and additiopn reactions

Togo, Hideo,Taguchi, Rie,Yamaguchi, Kentaro,Yoikoyama, Masataka

, p. 2135 - 2140 (2007/10/02)

The reactivity of arenes with 4-methylquinoline (substitution) as a typical heteroaromatic base and phenyl vinyl sulfone (addition) as a typical activated olefin has been studied under thermal and irradiation conditions.The results suggest that electron-withdrawing groups on the aromatic ring in arenes are detrimental to reactions.The crystal structures of arenes 10 and 1e are reported.

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 80859-83-2