Welcome to LookChem.com Sign In|Join Free
  • or
2,2'-BI(1,8-NAPHTHYRIDINE), also known as dipyridyl, is a chemical compound characterized by two pyridine rings linked by a single bond at the 2 and 2' positions. It is recognized for its role as a ligand in coordination chemistry, where it forms complexes with various metal ions. 2,2'-BI(1,8-NAPHTHYRIDINE) is notable for its applications in the development of new coordination compounds, catalysis, and in the production of advanced electronic devices such as organic light-emitting diodes (OLEDs). Furthermore, 2,2'-BI(1,8-NAPHTHYRIDINE) holds promise in medicinal chemistry due to its distinctive chemical structure and its capacity to engage with biological systems.

69110-33-4

Post Buying Request

69110-33-4 Suppliers

Recommended suppliers

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

69110-33-4 Usage

Uses

Used in Coordination Chemistry:
2,2'-BI(1,8-NAPHTHYRIDINE) is used as a ligand for forming complexes with different metal ions, which is crucial in the study and application of coordination chemistry. Its ability to chelate metals allows for the development of new compounds with specific properties and applications.
Used in Catalyst Development:
In the field of catalysis, 2,2'-BI(1,8-NAPHTHYRIDINE) is utilized as a component in the creation of catalysts that can accelerate chemical reactions. Its presence in these catalysts can enhance reaction rates and selectivity, making industrial processes more efficient.
Used in Electronics Manufacturing:
2,2'-BI(1,8-NAPHTHYRIDINE) is used as a component in the manufacture of electronic devices, particularly organic light-emitting diodes (OLEDs). Its role in these devices contributes to their performance, including aspects such as luminance and energy efficiency.
Used in Medicinal Chemistry:
2,2'-BI(1,8-NAPHTHYRIDINE) is employed in medicinal chemistry for its potential to interact with biological systems. Its unique structure allows it to be a candidate for the development of new pharmaceuticals, particularly those that require specific binding properties with biological targets.

Check Digit Verification of cas no

The CAS Registry Mumber 69110-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69110-33:
(7*6)+(6*9)+(5*1)+(4*1)+(3*0)+(2*3)+(1*3)=114
114 % 10 = 4
So 69110-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H10N4/c1-3-11-5-7-13(19-15(11)17-9-1)14-8-6-12-4-2-10-18-16(12)20-14/h1-10H

69110-33-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B1423)  2,2'-Bi(1,8-naphthyridine)  

  • 69110-33-4

  • 100mg

  • 1,450.00CNY

  • Detail

69110-33-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-Bi(1,8-naphthyridine)

1.2 Other means of identification

Product number -
Other names 2-(1,8-naphthyridin-2-yl)-1,8-naphthyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69110-33-4 SDS

69110-33-4Downstream Products

69110-33-4Relevant academic research and scientific papers

One-pot homo- and cross-coupling of diazanaphthalenes via C-H substitution: Synthesis of Bis- and Tris-diazanaphthalenes

Ucar, Sefa,Dastan, Arif

, p. 4013 - 4022 (2020/09/21)

The transition metal-free coupling reactions of unactivated diazanaphthalenes were studied using only lithium tetramethylpiperidine (LiTMP) reagent. Symmetrical and nonsymmetrical bis-diazanaphthalenes were synthesized in moderate to high yield by homo- and cross-coupling of related monomers. In addition, the single-step synthesis of diquinoxalino [2,3-a: 2', 3'c] phenazine and 2,2': 3', 2″ - terquinoxaline using the appropriate equivalent amount of LiTMP was performed. The products were characterized by means of NMR spectroscopy and HRMS spectrometry.

Polyaza Cavity Shaped Molecules. Annelated Derivatives of 2-(2'-Pyridyl)-1,8-naphthyridine and 2,2'-Bi-1,8-naphthyridine

Thummel, Randolph P.,Lefoulon, Francois,Cantu, David,Mahadevan, Ramanathan

, p. 2208 - 2212 (2007/10/02)

A two-step method is presented for the oxidation of the 2-methylene position of 2,3-cycloalkenopyridines.The pyridyl ketones thus obtained may be reacted with 2-aminonicotinaldehyde to yield 3,3'-annelated derivatives of 2-(2'-pyridyl)-1,8-naphthyridine.T

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 69110-33-4