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2-(pyridin-3-yl)pyridin-3-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 170808-76-1 Structure
  • Basic information

    1. Product Name: 2-(pyridin-3-yl)pyridin-3-amine
    2. Synonyms: 2-(pyridin-3-yl)pyridin-3-amine;[2,3-bipyridin]-3-amine
    3. CAS NO:170808-76-1
    4. Molecular Formula: C10H9N3
    5. Molecular Weight: 171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 170808-76-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(pyridin-3-yl)pyridin-3-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(pyridin-3-yl)pyridin-3-amine(170808-76-1)
    11. EPA Substance Registry System: 2-(pyridin-3-yl)pyridin-3-amine(170808-76-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 170808-76-1(Hazardous Substances Data)

170808-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 170808-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,8,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 170808-76:
(8*1)+(7*7)+(6*0)+(5*8)+(4*0)+(3*8)+(2*7)+(1*6)=141
141 % 10 = 1
So 170808-76-1 is a valid CAS Registry Number.

170808-76-1Downstream Products

170808-76-1Relevant articles and documents

Etude du Comportement Photochimique de quelques Diaryl-1,3-triazenes

Julliard, Michel,Vernin, Gaston,Metzger, Jacques

, p. 456 - 466 (2007/10/02)

The photolysis of Diaryl-1,3-triazenes gives products whose structures are consistent with a cage recombination process of homolytically formed radicals and subsequent abstraction of hydrogen from the solvent molecules by arylamino radicals.In aromatic solvents, a free-radical chain process leads to the formation of products resulting from the homolytic substitution on the solvent.Quenching experiments show that singlet and triplet excited states are reactive but that intersystem crossing efficiency is low.

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