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53717-02-5

penta-O-acetyl-L-sorbose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53717-02-5 Structure

  • Basic information

    1. Product Name: penta-O-acetyl-L-sorbose
    2. Synonyms:
    3. CAS NO:53717-02-5
    4. Molecular Formula:
    5. Molecular Weight: 390.344
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53717-02-5.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: penta-O-acetyl-L-sorbose(CAS DataBase Reference)
    10. NIST Chemistry Reference: penta-O-acetyl-L-sorbose(53717-02-5)
    11. EPA Substance Registry System: penta-O-acetyl-L-sorbose(53717-02-5)

  • 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: 53717-02-5(Hazardous Substances Data)

53717-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53717-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,1 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53717-02:
(7*5)+(6*3)+(5*7)+(4*1)+(3*7)+(2*0)+(1*2)=115
115 % 10 = 5
So 53717-02-5 is a valid CAS Registry Number.

53717-02-5Relevant articles and documents

SYNTHESIS OF L-IDARO-1,4-LACTONE, AN INHIBITOR OF α-L-IDOSID-URONASE

Herd, J. Kenneth,Mayberry, William R.,Snell, Robert L.

, p. 33 - 40 (2007/10/02)

L-Idaro-1,4-lactone was synthesized by two different, published methods: (1) epimerization of monopotassium D-glucarate by refluxing in aqueous barium hydroxide, and (2) oxidation of L-iditol by heating in dilute nitric acid.The lactone, formed by heat dehydration from aqueous solution at low pH, was purified by paper chromatography, and quantitated by gas-liquid chromatography using inositol as the internal standard.The monolactone inhibited human, seminal-fluid α-L-idosiduronase activity, with either phenyl or 4-methylumbelliferyl α-L-idosiduronic acid as the substrate, to the same degree as D-glucaro-1,4-lactone inhibits α-D-glucosiduranose.

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