Welcome to LookChem.com Sign In|Join Free

CAS

  • or

128802-93-7

Post Buying Request

128802-93-7 Suppliers

Recommended suppliersmore

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

128802-93-7 Usage

General Description

2-(pyridin-3-ylmethyl)pyridine is a chemical compound with the molecular formula C11H10N2. It is a member of the pyridine family, which is a class of organic compounds that contain a six-membered ring with five carbon atoms and one nitrogen atom. This specific compound consists of two pyridine rings with a methyl group attached to the third position of one of the rings. It is used in the pharmaceutical industry as a building block for the synthesis of various drug compounds and in research as a reagent in organic synthesis. It is also utilized in the production of specialty chemicals and agrochemicals. Additionally, it may have potential applications in the field of material science.

Check Digit Verification of cas no

The CAS Registry Mumber 128802-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,0 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 128802-93:
(8*1)+(7*2)+(6*8)+(5*8)+(4*0)+(3*2)+(2*9)+(1*3)=137
137 % 10 = 7
So 128802-93-7 is a valid CAS Registry Number.

128802-93-7Downstream Products

128802-93-7Relevant articles and documents

Versatile C(sp2)?C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes

Dean, William M.,?iau?iulis, Mindaugas,Storr, Thomas E.,Lewis, William,Stockman, Robert A.

, p. 10013 - 10016 (2016/08/16)

The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.

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

What can I do for you?
Get Best Price

Get Best Price for 128802-93-7