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72974-68-6

trans-4-hydroxy-3-(3'-hydroxyoct-1'-enyl)cyclopent-1-ene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72974-68-6 Structure

  • Basic information

    1. Product Name: trans-4-hydroxy-3-(3'-hydroxyoct-1'-enyl)cyclopent-1-ene
    2. Synonyms:
    3. CAS NO:72974-68-6
    4. Molecular Formula:
    5. Molecular Weight: 210.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72974-68-6.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: trans-4-hydroxy-3-(3'-hydroxyoct-1'-enyl)cyclopent-1-ene(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-4-hydroxy-3-(3'-hydroxyoct-1'-enyl)cyclopent-1-ene(72974-68-6)
    11. EPA Substance Registry System: trans-4-hydroxy-3-(3'-hydroxyoct-1'-enyl)cyclopent-1-ene(72974-68-6)

  • 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: 72974-68-6(Hazardous Substances Data)

72974-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72974-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,7 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72974-68:
(7*7)+(6*2)+(5*9)+(4*7)+(3*4)+(2*6)+(1*8)=166
166 % 10 = 6
So 72974-68-6 is a valid CAS Registry Number.

72974-68-6Relevant articles and documents

Photolytic Conversion of Some Bicycloheptanones into 3-Hydroxy- or 3-Methoxy-2-oxabicyclooctan-2-ones

Newton, Roger F.,Reynolds, Derek P.,Crossland, Noelle M.,Kelly, David R.,Roberts, Stanley M.

, p. 1583 - 1586 (2007/10/02)

The ketones (1) and (7)-(9) gave the corresponding cyclic acetals (3), (4), and (12)-(17), respectively, on photolysis in methanol.Concurrent production of the alkenes (6) and (18)-(20) detracted from the potential synthetic utility of this process.However, photolysis of the ketones (8), (10), and (11) in aqueous tetrahydrofuran or aqueous acetonitrile led to a highly selective ring-expansion process, and consequently high yields of the corresponding γ-lactols (21)-(23).

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