Welcome to LookChem.com Sign In|Join Free
  • or
Benzaldehyde, 2,2'-(1,4-piperazinediyl)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112253-19-7

Post Buying Request

112253-19-7 Suppliers

Recommended suppliers

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

112253-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112253-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,5 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112253-19:
(8*1)+(7*1)+(6*2)+(5*2)+(4*5)+(3*3)+(2*1)+(1*9)=77
77 % 10 = 7
So 112253-19-7 is a valid CAS Registry Number.

112253-19-7Downstream Products

112253-19-7Relevant academic research and scientific papers

Synthesis and characterization of Co(II), Ni(II), Zn(II) and Cu(II) complexes with a new tetraazamacrocyclic Schiff base ligand containing a piperazine moiety: X-ray crystal structure determination of the Co(II) complex

Keypour, Hassan,Rahpeyma, Nasibeh,Arzhangi, Parisa,Rezaeivala, Majid,Elerman, Yalcin,Buyukgungor, Orhan,Valencia, Laura

, p. 1144 - 1148 (2010)

Two macrocyclic Schiff base ligands, L1 [1+1] and L2 [2+2], have been obtained in a one-pot cyclocondensation of 1,4-bis(2-formylphenyl)piperazine and 1,3-diaminopropane. Unfortunately, because of the low solubility of both ligands,

Diastereoselective Bidirectional C(sp3)?H Bond Functionalization of Piperazine Compounds

Kwok Chan, Wesley Ting,Law, Ga-Lai,Yeung, Chi-Tung,Zhou, Xiao-Le

supporting information, (2022/01/11)

A highly diastereoselective bidirectional C(sp3)?H bond functionalization of piperazine compounds, triggered by a Lewis acid catalyzed sequential hydride shift/cyclization process, is reported. Catalysts and ligands are key factors that control the diastereoselectivity of the reaction. The reaction affords the product with good yield and high diastereoselectivity. Detailed investigation of the reaction mechanism reveals that the energy barrier between the cis products and trans products results in the diastereoselectivity of the reaction. The trans products, which have higher energy and which are generated from the cis products, act as intermediate products. (Figure presented.).

A Novel Two-Step Synthesis of Hexahydropyrazinoquinolines

Nijhuis, Walter H. N.,Verboom, Willem,Reinhoudt, David N.

, p. 641 - 645 (2007/10/02)

The hexahydropyrazinoquinolines 2 were prepared in good yields by reaction of 2-(4-substituted 1-piperazinyl)benzaldehydes 5 with malononitrile and subsequent thermal cyclization of the condensation products 6; the latter reaction takes place via a

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 112253-19-7