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CAS

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1020267-39-3

methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1020267-39-3 Structure

  • Basic information

    1. Product Name: methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate
    2. Synonyms: methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate
    3. CAS NO:1020267-39-3
    4. Molecular Formula:
    5. Molecular Weight: 308.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1020267-39-3.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: methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate(1020267-39-3)
    11. EPA Substance Registry System: methyl (2R,4S,6R)-[6-(2-benzyloxyethyl)-4-hydroxy-tetrahydropyran-2-yl]acetate(1020267-39-3)

  • 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: 1020267-39-3(Hazardous Substances Data)

1020267-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1020267-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,2,6 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1020267-39:
(9*1)+(8*0)+(7*2)+(6*0)+(5*2)+(4*6)+(3*7)+(2*3)+(1*9)=93
93 % 10 = 3
So 1020267-39-3 is a valid CAS Registry Number.

1020267-39-3Relevant articles and documents

Total synthesis of the marine metabolite (-)-clavosolide D

Seden, Peter T.,Charmant, Jonathan P. H.,Willis, Christine L.

, p. 1637 - 1640 (2008)

The first total synthesis of the marine natural product (-)-clavosolide D is described confirming the structure of the unsymmetrical 16- membered diolide glycosylated by permethylated D-xylose moieties. Following efficient assembly of the two tetrahydropyrans using stereoselective Prins cyclizations, the side chains were introduced via an allylation/isomerization/anti cyclopropanation sequence; the final macrolactonization step was achieved under Yamaguchi conditions.2008 American Chemical Society.

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