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CAS

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80536-42-1

2-(5-Pentyl-isoxazol-3-yl)-1-phenyl-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80536-42-1 Structure

  • Basic information

    1. Product Name: 2-(5-Pentyl-isoxazol-3-yl)-1-phenyl-ethanol
    2. Synonyms:
    3. CAS NO:80536-42-1
    4. Molecular Formula:
    5. Molecular Weight: 259.348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80536-42-1.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-(5-Pentyl-isoxazol-3-yl)-1-phenyl-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(5-Pentyl-isoxazol-3-yl)-1-phenyl-ethanol(80536-42-1)
    11. EPA Substance Registry System: 2-(5-Pentyl-isoxazol-3-yl)-1-phenyl-ethanol(80536-42-1)

  • 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: 80536-42-1(Hazardous Substances Data)

80536-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80536-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80536-42:
(7*8)+(6*0)+(5*5)+(4*3)+(3*6)+(2*4)+(1*2)=121
121 % 10 = 1
So 80536-42-1 is a valid CAS Registry Number.

80536-42-1Downstream Products

80536-42-1Relevant articles and documents

ISOXAZOLES AS 4b-DIKETONE SYNTHONS-SELECTIVE ANION FORMATION ON 3,5-DIALKYLISOXAZOLES

Brunelle, D. J.

, p. 3699 - 3702 (1981)

3,5-Dimethylisoxazole can be metalated and alkylated regiospecifically.Alkylation occurs first on the 5-methyl group, and a second alkylation occurs on the 3-methyl group.This method permits specific synthesis of disubstituted isoxazoles, and of the corresponding β-diketones.

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