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3,4'-Bipyridin-2'-amine, also known as 2-Amino-3,4'-bipyridine, is an aromatic amine chemical compound characterized by two pyridine rings connected by a carbon-carbon bond at the 3 and 4 positions. It is recognized for its unique structural and reactivity properties, which make it a valuable building block in organic synthesis and chemical research. Its ability to form metal complexes also renders it useful in coordination chemistry.

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  • 865604-20-2 Structure
  • Basic information

    1. Product Name: 3,4'-BIPYRIDIN-2'-AMINE
    2. Synonyms: [3,4'-bipyridin]-2'-amine; 3,4'-Bipyridin-2'-amine
    3. CAS NO:865604-20-2
    4. Molecular Formula: C10H9N3
    5. Molecular Weight: 171.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 865604-20-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 371.9°C at 760 mmHg
    3. Flash Point: 206.5°C
    4. Appearance: /
    5. Density: 1.193g/cm3
    6. Vapor Pressure: 9.95E-06mmHg at 25°C
    7. Refractive Index: 1.633
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,4'-BIPYRIDIN-2'-AMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,4'-BIPYRIDIN-2'-AMINE(865604-20-2)
    12. EPA Substance Registry System: 3,4'-BIPYRIDIN-2'-AMINE(865604-20-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 865604-20-2(Hazardous Substances Data)

865604-20-2 Usage

Uses

Used in Organic Synthesis:
3,4'-Bipyridin-2'-amine is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure and reactivity properties facilitate the creation of a wide range of molecules with potential applications in different fields.
Used in Pharmaceutical Development:
This chemical compound is utilized as a starting material in the development of new pharmaceuticals. Its potential use in medicine is attributed to its ability to form metal complexes, which can be harnessed to create drugs with specific therapeutic properties.
Used in Coordination Chemistry:
3,4'-Bipyridin-2'-amine is used as a ligand in coordination chemistry to form metal complexes. These complexes have potential applications in various areas, including catalysis, materials science, and the development of new technologies.
Used in Research and Development:
As a building block in chemical research, 3,4'-Bipyridin-2'-amine is instrumental in the exploration of new chemical reactions and the synthesis of novel compounds. Its unique properties make it a valuable tool for scientists working on the cutting edge of chemical and materials research.

Check Digit Verification of cas no

The CAS Registry Mumber 865604-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,6,0 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 865604-20:
(8*8)+(7*6)+(6*5)+(5*6)+(4*0)+(3*4)+(2*2)+(1*0)=182
182 % 10 = 2
So 865604-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3/c11-10-6-8(3-5-13-10)9-2-1-4-12-7-9/h1-7H,(H2,11,13)

865604-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4'-Bipyridin-2'-amine

1.2 Other means of identification

Product number -
Other names [3,4']bipyridinyl-2'-ylamine

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:865604-20-2 SDS

865604-20-2Downstream Products

865604-20-2Relevant articles and documents

DNA gyrase (GyrB)/topoisomerase IV (ParE) inhibitors: Synthesis and antibacterial activity

East, Stephen P.,White, Clara Bantry,Barker, Oliver,Barker, Stephanie,Bennett, James,Brown, David,Boyd, E. Andrew,Brennan, Christopher,Chowdhury, Chandana,Collins, Ian,Convers-Reignier, Emmanuelle,Dymock, Brian W.,Fletcher, Rowena,Haydon, David J.,Gardiner, Mihaly,Hatcher, Stuart,Ingram, Peter,Lancett, Paul,Mortenson, Paul,Papadopoulos, Konstantinos,Smee, Carol,Thomaides-Brears, Helena B.,Tye, Heather,Workman, James,Czaplewski, Lloyd G.

scheme or table, p. 894 - 899 (2009/08/15)

The synthesis and antibacterial activities of three chemotypes of DNA supercoiling inhibitors based on imidazolo[1,2-a]pyridine and [1,2,4]triazolo[1,5-a]pyridine scaffolds that target the ATPase subunits of DNA gyrase and topoisomerase IV (GyrB/ParE) is reported. The most potent scaffold was selected for optimization leading to a series with potent Gram-positive antibacterial activity and a low resistance frequency.

IMIDAZO[1,2-A]PYRIDINE COMPOUNDS AS RECEPTOR TYROSINE KINASE INHIBITORS

-

Page/Page column 59, (2008/12/04)

Compounds of Formula (I) in which A, B, R1, R1a, R2, R3, R4, R5, R6, R7 and R8 have the meanings given in the specification, are receptor tyrosine inhibitors useful in the treatment of diseases mediated by class 3 and class 5 receptor tyrosine kinases. Particular compounds of this invention have also been found to be inhibitors of Pim-1

New catalysts for Suzuki-Miyaura coupling reactions of heteroatom- substituted heteroaryl chlorides

Guram, Anil S.,Wang, Xiang,Bunel, Emilio E.,Faul, Margaret M.,Larsen, Robert D.,Martinelli, Michael J.

, p. 5104 - 5112 (2008/02/07)

(Chemical Equation Presented) The new air-stable PdCl2{PR 2(Ph-R′)}2 complexes, readily prepared from commercial reagents, exhibit unique efficiency as catalysts for the Suzuki-Miyaura coupling reactions of a variety of he

IMIDAZOPYRIDINE AND IMIDAZOPYRIMIDINE DERIVATIVES AS ANTIBACTERIAL AGENTS

-

Page/Page column 32, (2008/06/13)

Compounds of formula I and methods for their preparation are disclosed. Further disclosed are methods of making biologically active compounds of formula I as well as pharmaceutically acceptable compositions comprising compounds of formula I. Compounds of

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