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CAS

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1352548-05-0

2-(4-chloro-2-nitrophenyl)-5-ethylfuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352548-05-0 Structure

  • Basic information

    1. Product Name: 2-(4-chloro-2-nitrophenyl)-5-ethylfuran
    2. Synonyms: 2-(4-chloro-2-nitrophenyl)-5-ethylfuran
    3. CAS NO:1352548-05-0
    4. Molecular Formula:
    5. Molecular Weight: 251.669
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352548-05-0.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-chloro-2-nitrophenyl)-5-ethylfuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-chloro-2-nitrophenyl)-5-ethylfuran(1352548-05-0)
    11. EPA Substance Registry System: 2-(4-chloro-2-nitrophenyl)-5-ethylfuran(1352548-05-0)

  • 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: 1352548-05-0(Hazardous Substances Data)

1352548-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352548-05-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,5,4 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1352548-05:
(9*1)+(8*3)+(7*5)+(6*2)+(5*5)+(4*4)+(3*8)+(2*0)+(1*5)=150
150 % 10 = 0
So 1352548-05-0 is a valid CAS Registry Number.

1352548-05-0Relevant articles and documents

Furan ring opening-indole ring closure: Recyclization of 2-(2-aminophenyl)furans into 2-(2-oxoalkyl)indoles

Pilipenko, Arkady S.,Mel'Chin, Vladimir V.,Trushkov, Igor V.,Cheshkov, Dmitry A.,Butin, Alexander V.

supporting information; experimental part, p. 619 - 627 (2012/01/05)

The acid-catalyzed rearrangement of 5-alkyl-2-[2-(sulfonylamino)phenyl] furans into 2-(2-oxoalkyl)indoles is described. When the N-sulfonyl group in the starting compounds was displaced by an N-acyl group, the corresponding indoles were not formed under t

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