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917967-39-6

C26H41NO3Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 917967-39-6 Structure

  • Basic information

    1. Product Name: C26H41NO3Si
    2. Synonyms: C26H41NO3Si
    3. CAS NO:917967-39-6
    4. Molecular Formula:
    5. Molecular Weight: 443.702
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 917967-39-6.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: C26H41NO3Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H41NO3Si(917967-39-6)
    11. EPA Substance Registry System: C26H41NO3Si(917967-39-6)

  • 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: 917967-39-6(Hazardous Substances Data)

917967-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917967-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,9,6 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 917967-39:
(8*9)+(7*1)+(6*7)+(5*9)+(4*6)+(3*7)+(2*3)+(1*9)=226
226 % 10 = 6
So 917967-39-6 is a valid CAS Registry Number.

917967-39-6Downstream Products

917967-39-6Relevant articles and documents

Synthesis and biological evaluation of dihydrofuran-fused perhydrophenanthrenes as a new anti-influenza agent having novel structural characteristic

Matsuya, Yuji,Sasaki, Kazushige,Ochiai, Hiroshi,Nemoto, Hideo

, p. 424 - 432 (2007)

Dihydrofuran-fused perhydrophenanthrenes were synthesized by means of o-quinodimethane chemistry with high generality and stereoselectivity, and found to exhibit potent anti-influenza activity. These compounds exerted an inhibitory effect on various strains of influenza virus growth, including influenza A and B, with a concentration dependent manner, and direct cytotoxicity was low. Several biological experiments suggested that these new drugs affected a virus replication process before mRNA synthesis stage. Novel rigid cage-type of structural characteristic of the compounds has not been found in hitherto anti-influenza drugs, and will provide new basis and motif for exploring promising and unprecedented anti-influenza agents.

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