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449753-95-1

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  • 449753-95-1 Structure

  • Basic information

    1. Product Name: rac-3-(benzoyloxy)hept-1-yne
    2. Synonyms: rac-3-(benzoyloxy)hept-1-yne
    3. CAS NO:449753-95-1
    4. Molecular Formula:
    5. Molecular Weight: 216.28
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 449753-95-1.mol
    9. Article Data: 2

  • 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-3-(benzoyloxy)hept-1-yne(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-3-(benzoyloxy)hept-1-yne(449753-95-1)
    11. EPA Substance Registry System: rac-3-(benzoyloxy)hept-1-yne(449753-95-1)

  • 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: 449753-95-1(Hazardous Substances Data)

449753-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 449753-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,7,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 449753-95:
(8*4)+(7*4)+(6*9)+(5*7)+(4*5)+(3*3)+(2*9)+(1*5)=201
201 % 10 = 1
So 449753-95-1 is a valid CAS Registry Number.

449753-95-1Relevant articles and documents

A simple method for the preparation of (5Z,8Z,11Z,14Z)-16-Hydroxyeicosa-5,8,11,14-tetraenoic acid enantiomers and the corresponding 14,15-Dehydro analogues: Role of the 16-Hydroxy group for the lipoxygenase reaction

Ivanov, Igor V.,Romanov, Stepan G.,Groza, Nataliya V.,Nigam, Santosh,Kuhn, Hartmut,Myagkova, Galina I.

, p. 2335 - 2343 (2002)

(5Z,8Z,11Z,13E)-15-Hydroxy-5,8,11,13-eicosatetraenoic acid (15-HETE) is not well oxygenated by arachidonate 15-lipoxygenases because of two structural reasons: (i) it contains a hydrophilic OH-group in close proximity to its methyl end and (ii) it lacks t

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