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115482-99-0

(2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115482-99-0 Structure

  • Basic information

    1. Product Name: (2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol
    2. Synonyms: (2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol
    3. CAS NO:115482-99-0
    4. Molecular Formula:
    5. Molecular Weight: 390.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115482-99-0.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: (2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol(115482-99-0)
    11. EPA Substance Registry System: (2R,3R)-5-O-benzyl-3-vinyl-1-O-tosyl-1,2,5-pentanetriol(115482-99-0)

  • 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: 115482-99-0(Hazardous Substances Data)

115482-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115482-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,8 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115482-99:
(8*1)+(7*1)+(6*5)+(5*4)+(4*8)+(3*2)+(2*9)+(1*9)=130
130 % 10 = 0
So 115482-99-0 is a valid CAS Registry Number.

115482-99-0Relevant articles and documents

Asymmetric Synthesis of Carbacyclin Precursors by Pauson-Khand Cyclization

Mulzer, Johann,Graske, Klaus-Dieter,Kirste, Burkhard

, p. 891 - 898 (2007/10/02)

The carbacyclin precursors 11, 17, 18 have been prepared from the en-ynes 10, 15, 16 by cobalt-mediated cyclization (Pauson-Khand reaction) with varying degrees of diastereoselectivity.

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