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CAS

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696664-22-9

2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 696664-22-9 Structure

  • Basic information

    1. Product Name: 2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline
    2. Synonyms: 2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline
    3. CAS NO:696664-22-9
    4. Molecular Formula:
    5. Molecular Weight: 369.463
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 696664-22-9.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: 2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline(696664-22-9)
    11. EPA Substance Registry System: 2-(3'-benzyloxy-4'-methoxyphenethyl)quinoline(696664-22-9)

  • 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: 696664-22-9(Hazardous Substances Data)

696664-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 696664-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,6,6 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 696664-22:
(8*6)+(7*9)+(6*6)+(5*6)+(4*6)+(3*4)+(2*2)+(1*2)=219
219 % 10 = 9
So 696664-22-9 is a valid CAS Registry Number.

696664-22-9Relevant articles and documents

The enantioselective total synthesis of alkaloid (-)-galipeine

Yang, Peng-Yu,Zhou, Yong-Gui

, p. 1145 - 1149 (2004)

The first total synthesis of (-)-galipeine was accomplished in seven steps with 54% overall yield from isovanillin based on Ir-catalyzed asymmetric hydrogenation of a quinoline derivative as a key step, with its absolute stereochemistry being established.

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