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1393478-29-9

C26H35IO5Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393478-29-9 Structure

  • Basic information

    1. Product Name: C26H35IO5Si
    2. Synonyms: C26H35IO5Si
    3. CAS NO:1393478-29-9
    4. Molecular Formula:
    5. Molecular Weight: 582.551
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393478-29-9.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: C26H35IO5Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C26H35IO5Si(1393478-29-9)
    11. EPA Substance Registry System: C26H35IO5Si(1393478-29-9)

  • 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: 1393478-29-9(Hazardous Substances Data)

1393478-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393478-29-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,4,7 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1393478-29:
(9*1)+(8*3)+(7*9)+(6*3)+(5*4)+(4*7)+(3*8)+(2*2)+(1*9)=199
199 % 10 = 9
So 1393478-29-9 is a valid CAS Registry Number.

1393478-29-9Relevant articles and documents

A chiron approach to aminocytitols by petasis-borono-mannich reaction: Formal synthesis of (+)-conduramine e and (-)-conduramine e

Ghosal, Partha,Shaw, Arun K.

, p. 7627 - 7632,6 (2012)

A chiron approach to a stereoselective route for the synthesis of aminocytitols from carbohydrates is described. The formal synthesis of (+)-conduramine E and (-)-conduramine E was achieved by utilizing this strategy. The key features of the synthetic strategy include one-pot three-component Petasis-Borono-Mannich reaction to introduce the syn-β-amino alcohol functionality of conduramine E and ring-closing metathesis to construct its carbocyclic core. The present synthetic approach paves the way for stereoselective synthesis of several conduramines starting from carbohydrates.

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