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bis(5-methoxypyridin-3-yl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1445972-34-8 Structure
  • Basic information

    1. Product Name: bis(5-methoxypyridin-3-yl)amine
    2. Synonyms:
    3. CAS NO:1445972-34-8
    4. Molecular Formula:
    5. Molecular Weight: 231.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1445972-34-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: bis(5-methoxypyridin-3-yl)amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(5-methoxypyridin-3-yl)amine(1445972-34-8)
    11. EPA Substance Registry System: bis(5-methoxypyridin-3-yl)amine(1445972-34-8)
  • 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: 1445972-34-8(Hazardous Substances Data)

1445972-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1445972-34-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,9,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1445972-34:
(9*1)+(8*4)+(7*4)+(6*5)+(5*9)+(4*7)+(3*2)+(2*3)+(1*4)=188
188 % 10 = 8
So 1445972-34-8 is a valid CAS Registry Number.

1445972-34-8Upstream product

1445972-34-8Downstream Products

1445972-34-8Relevant articles and documents

Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts

Cheung, Chi Wai,Surry, David S.,Buchwald, Stephen L.

supporting information, p. 3734 - 3737 (2013/08/23)

A method for the Pd-catalyzed arylation of ammonia with a wide range of aryl and heteroaryl halides, including challenging five-membered heterocyclic substrates, is described. Excellent selectivity for monoarylation of ammonia to primary arylamines was achieved under mild conditions or at rt by the use of bulky biarylphosphine ligands (L6, L7, and L4) as well as their corresponding aminobiphenyl palladacycle precatalysts (3a, 3b, and 3c). As this process requires neither the use of a glovebox nor high pressures of ammonia, it should be widely applicable.

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