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CAS

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1013026-48-6

5,6-dimethoxy-5,6-dimethyl[1,4]dioxan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1013026-48-6 Structure

  • Basic information

    1. Product Name: 5,6-dimethoxy-5,6-dimethyl[1,4]dioxan-2-one
    2. Synonyms:
    3. CAS NO:1013026-48-6
    4. Molecular Formula:
    5. Molecular Weight: 190.196
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1013026-48-6.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: 5,6-dimethoxy-5,6-dimethyl[1,4]dioxan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,6-dimethoxy-5,6-dimethyl[1,4]dioxan-2-one(1013026-48-6)
    11. EPA Substance Registry System: 5,6-dimethoxy-5,6-dimethyl[1,4]dioxan-2-one(1013026-48-6)

  • 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: 1013026-48-6(Hazardous Substances Data)

1013026-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1013026-48-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,3,0,2 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1013026-48:
(9*1)+(8*0)+(7*1)+(6*3)+(5*0)+(4*2)+(3*6)+(2*4)+(1*8)=76
76 % 10 = 6
So 1013026-48-6 is a valid CAS Registry Number.

1013026-48-6Downstream Products

1013026-48-6Relevant articles and documents

A highly diastereoselective synthesis of α-hydroxy-β-amino acid derivatives via a Lewis acid catalyzed three-component condensation reaction

Gassa, Federico,Contini, Alessandro,Fontana, Gabriele,Pellegrino, Sara,Gelmi, Maria Luisa

, p. 7099 - 7106 (2010)

A very efficient three-component synthesis of a series of syn α-hydroxy-β-amino esters, obtained in high diastereoselection and yield, was realized starting from an aldehyde, benzylamine, and the ketene silyl acetals derived from Ley's lactones. The synthetic protocol was optimized and the above compounds were obtained without the isolation of intermediates. The origin of the observed diastereoselection was investigated through a computational model of the key reaction step.

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