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  • 1394910-09-8 Structure
  • Basic information

    1. Product Name: C45H54F6O11
    2. Synonyms:
    3. CAS NO:1394910-09-8
    4. Molecular Formula:
    5. Molecular Weight: 884.908
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1394910-09-8.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: C45H54F6O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C45H54F6O11(1394910-09-8)
    11. EPA Substance Registry System: C45H54F6O11(1394910-09-8)
  • 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: 1394910-09-8(Hazardous Substances Data)

1394910-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1394910-09-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,9,1 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1394910-09:
(9*1)+(8*3)+(7*9)+(6*4)+(5*9)+(4*1)+(3*0)+(2*0)+(1*9)=178
178 % 10 = 8
So 1394910-09-8 is a valid CAS Registry Number.

1394910-09-8Downstream Products

1394910-09-8Relevant articles and documents

A novel tricyclic polyketide and its biosynthetic precursor azaphilone derivatives from the endophytic fungus Dothideomycete sp

Senadeera, Sarath P. D.,Wiyakrutta, Suthep,Mahidol, Chulabhorn,Ruchirawat, Somsak,Kittakoop, Prasat

, p. 7220 - 7226 (2012)

Azaphilone derivatives 1 and 2 and a novel tricyclic polyketide 3, together with a known azaphilone, austdiol (4), were isolated from the endophytic fungus Dothideomycete sp., which was isolated from a Thai medicinal plant, Tiliacora triandra. Compound 3 is the first polyketide having a tricyclic 6,6,6 ring system, which is similar to that of a terpenoid skeleton. The absolute configurations of stereogenic centers in 1-3 were addressed by Mosher's method and biosynthetic analogy with a known azaphilone isolated from the same fungus. Cytotoxic and antimicrobial activities of the isolated compounds were evaluated.

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