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CAS

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1440513-49-4

6,7-dimethoxy-1-(1-nitropropyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1440513-49-4 Structure

  • Basic information

    1. Product Name: 6,7-dimethoxy-1-(1-nitropropyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline
    2. Synonyms:
    3. CAS NO:1440513-49-4
    4. Molecular Formula:
    5. Molecular Weight: 356.422
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1440513-49-4.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: 6,7-dimethoxy-1-(1-nitropropyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6,7-dimethoxy-1-(1-nitropropyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline(1440513-49-4)
    11. EPA Substance Registry System: 6,7-dimethoxy-1-(1-nitropropyl)-2-phenyl-1,2,3,4-tetrahydroisoquinoline(1440513-49-4)

  • 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: 1440513-49-4(Hazardous Substances Data)

1440513-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440513-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,5,1 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1440513-49:
(9*1)+(8*4)+(7*4)+(6*0)+(5*5)+(4*1)+(3*3)+(2*4)+(1*9)=124
124 % 10 = 4
So 1440513-49-4 is a valid CAS Registry Number.

1440513-49-4Downstream Products

1440513-49-4Relevant articles and documents

Transition metal-free α-C(sp3)-H bond functionalization of amines by oxidative cross dehydrogenative coupling reaction: Simple and direct access to C-4-alkylated 3,4-dihydroquinazoline derivatives

Kumar, R. Arun,Saidulu,Prasad, K. Rajendra,Kumar, G. Sathish,Sridhar,Reddy, K. Rajender

supporting information, p. 2985 - 2991 (2013/01/15)

A transition metal-free catalytic system has been developed for the cross dehydrogenative coupling of amines with nitroalkanes under mild condition employing potassium iodide/tert-butyl hydrogen peroxide catalytic system. This methodology was further extended for the construction of biologically important N-heterocycles, namely, 3,4-dihydroquinazoline derivatives. This novel strategy provides a simple, efficient, and direct access to 4-alkyl-3,4- dihydroquinazoline derivatives. Copyright

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