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1056395-61-9

1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1056395-61-9 Structure

  • Basic information

    1. Product Name: 1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline
    2. Synonyms: 1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline
    3. CAS NO:1056395-61-9
    4. Molecular Formula:
    5. Molecular Weight: 279.425
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1056395-61-9.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: 1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline(1056395-61-9)
    11. EPA Substance Registry System: 1-benzyl-2-butyl-1,2,3,4-tetrahydroquinoline(1056395-61-9)

  • 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: 1056395-61-9(Hazardous Substances Data)

1056395-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1056395-61-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,6,3,9 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1056395-61:
(9*1)+(8*0)+(7*5)+(6*6)+(5*3)+(4*9)+(3*5)+(2*6)+(1*1)=159
159 % 10 = 9
So 1056395-61-9 is a valid CAS Registry Number.

1056395-61-9Upstream product

1056395-61-9Downstream Products

1056395-61-9Relevant articles and documents

Rapid synthesis of the tetrahydroquinoline alkaloids: angustureine, cuspareine and galipinine

O'Byrne, Aisling,Evans, Paul

, p. 8067 - 8072 (2008)

A one-pot method for the preparation of 1,2-substituted dihydroquinolines is described. This method features the C-2 addition of a range of organolithium reagents to quinoline followed by the in-situ addition of an electrophile. Standard palladium-catalys

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