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1421504-06-4

2,4-dichloro-6-(furan-2-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1421504-06-4 Structure

  • Basic information

    1. Product Name: 2,4-dichloro-6-(furan-2-yl)aniline
    2. Synonyms: 2,4-dichloro-6-(furan-2-yl)aniline
    3. CAS NO:1421504-06-4
    4. Molecular Formula:
    5. Molecular Weight: 228.078
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1421504-06-4.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: 2,4-dichloro-6-(furan-2-yl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dichloro-6-(furan-2-yl)aniline(1421504-06-4)
    11. EPA Substance Registry System: 2,4-dichloro-6-(furan-2-yl)aniline(1421504-06-4)

  • 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: 1421504-06-4(Hazardous Substances Data)

1421504-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421504-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,5,0 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1421504-06:
(9*1)+(8*4)+(7*2)+(6*1)+(5*5)+(4*0)+(3*4)+(2*0)+(1*6)=104
104 % 10 = 4
So 1421504-06-4 is a valid CAS Registry Number.

1421504-06-4Relevant articles and documents

Synthesis of phenanthridine derivatives by microwave-mediated cyclization of o-furyl(allylamino)arenes

Read, Matthew Lovell,Gundersen, Lise-Lotte

, p. 1311 - 1316 (2013/03/29)

A novel and efficient synthesis of phenanthridines and aza analogues is reported. The key step is a microwave-mediated intramolecular Diels-Alder cyclization of o-furyl(allylamino)arenes. In the presence of a catalytic amount of acid, the DA-adduct reacts further to give the dihydrophenanthridines, which easily can be oxidized to fully aromatic compounds by air in the presence of UV light or by DDQ.

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