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CAS

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140381-68-6

Isoquinoline, 2-(5-fluoro-2-nitrophenyl)-1,2,3,4-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 140381-68-6 Structure

  • Basic information

    1. Product Name: Isoquinoline, 2-(5-fluoro-2-nitrophenyl)-1,2,3,4-tetrahydro-
    2. Synonyms:
    3. CAS NO:140381-68-6
    4. Molecular Formula: C15H13FN2O2
    5. Molecular Weight: 272.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 140381-68-6.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: Isoquinoline, 2-(5-fluoro-2-nitrophenyl)-1,2,3,4-tetrahydro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Isoquinoline, 2-(5-fluoro-2-nitrophenyl)-1,2,3,4-tetrahydro-(140381-68-6)
    11. EPA Substance Registry System: Isoquinoline, 2-(5-fluoro-2-nitrophenyl)-1,2,3,4-tetrahydro-(140381-68-6)

  • 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: 140381-68-6(Hazardous Substances Data)

140381-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140381-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,3,8 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 140381-68:
(8*1)+(7*4)+(6*0)+(5*3)+(4*8)+(3*1)+(2*6)+(1*8)=106
106 % 10 = 6
So 140381-68-6 is a valid CAS Registry Number.

140381-68-6Relevant articles and documents

Ring-opening Reactions of N-Aryl-1,2,3,4-tetrahydroisoquinoline Derivatives

Hedley, K. Andrew,Stanforth, Stephen P.

, p. 743 - 750 (2007/10/02)

The reaction of N-nitroaryl-1,2,3,4-tetrahydroisoquinolines 1a-e, 1g and 1j with N-bromosuccinimide (NBS) afforded aldehydes 3a-e, 3h and 3j respectively.N-(4-Nitrophenyl)-1-phenyl-1,2,3,4-tetrahydroisoquinoline 1n gave ketone 3n together with brominated product 3o when treated with NBS.

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