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1024613-11-3

(R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1024613-11-3 Structure

  • Basic information

    1. Product Name: (R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one
    2. Synonyms: (R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one
    3. CAS NO:1024613-11-3
    4. Molecular Formula:
    5. Molecular Weight: 320.504
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1024613-11-3.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: (R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one(1024613-11-3)
    11. EPA Substance Registry System: (R)-5-benzyl-5-(tert-butyldimethylsilyloxymethyl)dihydrofuran-2(3H)-one(1024613-11-3)

  • 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: 1024613-11-3(Hazardous Substances Data)

1024613-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1024613-11-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,4,6,1 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1024613-11:
(9*1)+(8*0)+(7*2)+(6*4)+(5*6)+(4*1)+(3*3)+(2*1)+(1*1)=93
93 % 10 = 3
So 1024613-11-3 is a valid CAS Registry Number.

1024613-11-3Relevant articles and documents

Asymmetric synthesis of 4′-C-benzyl-2′,3′-dideoxynucleoside analogues from 3-benzyl-2-hydroxy-2-cyclopenten-1-one

Jogi, Artur,Ilves, Marit,Paju, Anne,Pehk, Tonis,Kailas, Tiiu,Mueuerisepp, Aleksander-Mati,Lopp, Margus

, p. 628 - 634 (2008/09/19)

Both enantiomers of the key intermediate, 2-benzyl-5-oxo-tetrahydro-furan-2-carboxylic acid were obtained by asymmetric oxidation of 3-benzyl-2-hydroxy-2-cyclopenten-1-one with an ee ≥96%, using the tartaric ester/Ti(OiPr)4/t-BuOOH complex, and transformed to the corresponding 4′-substituted nucleoside analogues with up to 61% overall yield.

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