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1436417-40-1

C40H37NO6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1436417-40-1 Structure

  • Basic information

    1. Product Name: C40H37NO6
    2. Synonyms: C40H37NO6
    3. CAS NO:1436417-40-1
    4. Molecular Formula:
    5. Molecular Weight: 627.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1436417-40-1.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: C40H37NO6(CAS DataBase Reference)
    10. NIST Chemistry Reference: C40H37NO6(1436417-40-1)
    11. EPA Substance Registry System: C40H37NO6(1436417-40-1)

  • 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: 1436417-40-1(Hazardous Substances Data)

1436417-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1436417-40-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,6,4,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1436417-40:
(9*1)+(8*4)+(7*3)+(6*6)+(5*4)+(4*1)+(3*7)+(2*4)+(1*0)=151
151 % 10 = 1
So 1436417-40-1 is a valid CAS Registry Number.

1436417-40-1Relevant articles and documents

Total synthesis of dictyodendrins B and e

Liang, Jingjing,Hu, Weimin,Tao, Pengyu,Jia, Yanxing

, p. 5810 - 5815 (2013)

The concise synthesis of the novel telomerase inhibitors dictyodendrins B and E was completed in only 9 and 11 steps (longest linear sequence). The highly convergent strategy employed a palladium-catalyzed Larock indole synthesis and a palladium-mediated one-pot consecutive Buchwald-Hartwig amination/C-H activation reaction as key steps. The present synthesis exhibits respectable levels of atom-, redox-, and step-economy.

Total synthesis of dictyodendrins B and E, and formal synthesis of dictyodendrin C

Tao, Pengyu,Liang, Jingjing,Jia, Yanxing

, p. 5735 - 5748 (2014/11/07)

A full account of the concise total syntheses of dictyodendrins B and E, and the formal synthesis of dictyodendrin C are described. A palladium-catalysed Larock indole synthesis was used to form the highly substituted indole core, and a palladium-mediated

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