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213545-21-2

rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 213545-21-2 Structure

  • Basic information

    1. Product Name: rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol
    2. Synonyms: rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol
    3. CAS NO:213545-21-2
    4. Molecular Formula:
    5. Molecular Weight: 324.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 213545-21-2.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: rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol(213545-21-2)
    11. EPA Substance Registry System: rac-1-(benzoyloxy)tetradec-2(E)-ene-5,8-diyn-4-ol(213545-21-2)

  • 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: 213545-21-2(Hazardous Substances Data)

213545-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213545-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,5,4 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 213545-21:
(8*2)+(7*1)+(6*3)+(5*5)+(4*4)+(3*5)+(2*2)+(1*1)=102
102 % 10 = 2
So 213545-21-2 is a valid CAS Registry Number.

213545-21-2Relevant articles and documents

Synthetic research on hepoxilins. 7.* Divergent total synthesis of hepoxilins and related eicosanoids

Mel'nikova,Vasil'eva,Pivnitsky

, p. 1199 - 1208 (2007/10/03)

A new synthetic strategy for hydroxy-epoxy eicosanoids formed through the lipoxygenase pathway is developed. It makes use of a single synthon of the central functionalized fragment of the target molecules, namely racemic (E)-CICH2C≡CCHOHCH=CHCH2OBz. Elongation of the carbon chain of the synthon by successive condensations at both ends altenatively with hept-1-yne and hex-5-ynoic acid followed by enantioselective double bond epoxidation and partial hydrogenation of the triple bonds resulted in the syntheses of hepoxilins B3, their potential 8-lipoxygenase analogs, or their enantiomers, depending on the sequence of carbon chain elongations and the chirality of the epoxidation controller used.

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