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1335001-09-6

C37H36F6O11 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1335001-09-6 Structure

  • Basic information

    1. Product Name: C37H36F6O11
    2. Synonyms: C37H36F6O11
    3. CAS NO:1335001-09-6
    4. Molecular Formula:
    5. Molecular Weight: 770.677
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1335001-09-6.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: C37H36F6O11(CAS DataBase Reference)
    10. NIST Chemistry Reference: C37H36F6O11(1335001-09-6)
    11. EPA Substance Registry System: C37H36F6O11(1335001-09-6)

  • 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: 1335001-09-6(Hazardous Substances Data)

1335001-09-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1335001-09-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,5,0,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1335001-09:
(9*1)+(8*3)+(7*3)+(6*5)+(5*0)+(4*0)+(3*1)+(2*0)+(1*9)=96
96 % 10 = 6
So 1335001-09-6 is a valid CAS Registry Number.

1335001-09-6Downstream Products

1335001-09-6Relevant articles and documents

Dihydronaphthalenones from endophytic fungus Fusarium sp. BCC14842

Kornsakulkarn, Jittra,Dolsophon, Kulvadee,Boonyuen, Nattawut,Boonruangprapa, Tanapong,Rachtawee, Pranee,Prabpai, Samran,Kongsaeree, Palangpon,Thongpanchang, Chawanee

, p. 7540 - 7547 (2011)

Eleven new dihydronaphthalenones 1-11, together with five known compounds; 5-hydroxydihydrofusarubin C (12), javanicin, bostrycoidin, anhydrofusarubin, and 3-O-methylfusarubin, were isolated from the endophytic fungus Fusarium sp. BCC14842. Structures were elucidated by analyses of the NMR spectroscopic and mass spectrometry data. Javanicin, 3-O-methylfusarubin, compounds 3 and 7 exhibited antimycobacterial and cytotoxic activities. Javanicin also displayed antifungal activity with IC50 of 6.16 μg/mL, while compounds 2, 4, 5, 8, and 12 showed only cytotoxic activity.

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