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1571918-48-3

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  • 1571918-48-3 Structure

  • Basic information

    1. Product Name: N-((2R,3R,E)-3-hydroxy-1-((2-(hydroxymethyl)phenyl)thio)-octadec-4-en-2-yl)octanamide
    2. Synonyms: N-((2R,3R,E)-3-hydroxy-1-((2-(hydroxymethyl)phenyl)thio)-octadec-4-en-2-yl)octanamide
    3. CAS NO:1571918-48-3
    4. Molecular Formula:
    5. Molecular Weight: 547.886
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1571918-48-3.mol
    9. Article Data: 1

  • 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: N-((2R,3R,E)-3-hydroxy-1-((2-(hydroxymethyl)phenyl)thio)-octadec-4-en-2-yl)octanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-((2R,3R,E)-3-hydroxy-1-((2-(hydroxymethyl)phenyl)thio)-octadec-4-en-2-yl)octanamide(1571918-48-3)
    11. EPA Substance Registry System: N-((2R,3R,E)-3-hydroxy-1-((2-(hydroxymethyl)phenyl)thio)-octadec-4-en-2-yl)octanamide(1571918-48-3)

  • 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: 1571918-48-3(Hazardous Substances Data)

1571918-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1571918-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,9,1 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1571918-48:
(9*1)+(8*5)+(7*7)+(6*1)+(5*9)+(4*1)+(3*8)+(2*4)+(1*8)=193
193 % 10 = 3
So 1571918-48-3 is a valid CAS Registry Number.

1571918-48-3Downstream Products

1571918-48-3Relevant articles and documents

Aziridine ring opening for the synthesis of sphingolipid analogues: Inhibitors of sphingolipid-metabolizing enzymes

Alcaide, Anna,Llebaria, Amadeu

, p. 2993 - 3029 (2014/05/06)

A library of sphingolipid analogues is designed and tested as inhibitors against mammalian and fungal sphingolipid enzymes. The synthesis of sphingolipid analogues is based on the nucleophilic ring-opening reactions of N-activated aziridine derivatives wi

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