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1207067-85-3

4-(1-hydroxy-3-phenyl-2-propynyl)quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1207067-85-3 Structure

  • Basic information

    1. Product Name: 4-(1-hydroxy-3-phenyl-2-propynyl)quinoline
    2. Synonyms: 4-(1-hydroxy-3-phenyl-2-propynyl)quinoline
    3. CAS NO:1207067-85-3
    4. Molecular Formula:
    5. Molecular Weight: 259.307
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1207067-85-3.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: 4-(1-hydroxy-3-phenyl-2-propynyl)quinoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(1-hydroxy-3-phenyl-2-propynyl)quinoline(1207067-85-3)
    11. EPA Substance Registry System: 4-(1-hydroxy-3-phenyl-2-propynyl)quinoline(1207067-85-3)

  • 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: 1207067-85-3(Hazardous Substances Data)

1207067-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207067-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,0,6 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1207067-85:
(9*1)+(8*2)+(7*0)+(6*7)+(5*0)+(4*6)+(3*7)+(2*8)+(1*5)=133
133 % 10 = 3
So 1207067-85-3 is a valid CAS Registry Number.

1207067-85-3Downstream Products

1207067-85-3Relevant articles and documents

Preparation of some heterocyclic enones and ynones by isomerisation of the propargylic alcohols

Erenler, Ramazan,Uno, Masaharu,Goud, Thirumani Venkateshwar,Biellmanna, Jean-Francois

, p. 459 - 464 (2009)

The propargylic alcohols were synthesised by treatment of aldehydes with substituted acetylenes. The conversion of propargylic alcohols to propynones and propenones takes place with pyridine hydrochloride in methanol at room temperature. In presence of pyridinium triflate and p-toluenesulfonate the propynone was the only product isolated in the isomerisation of alcohol. The silylated propenone undergoes with cyclopentadiene a Diels-Alder cycloaddition to give ketone whose skeleton is related to that of quinine.

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