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CAS

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862546-71-2

4-hydroxy-5-trityloxymethyl-5H-furan-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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  • 862546-71-2 Structure

  • Basic information

    1. Product Name: 4-hydroxy-5-trityloxymethyl-5H-furan-2-one
    2. Synonyms: 4-hydroxy-5-trityloxymethyl-5H-furan-2-one
    3. CAS NO:862546-71-2
    4. Molecular Formula:
    5. Molecular Weight: 372.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 862546-71-2.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: 4-hydroxy-5-trityloxymethyl-5H-furan-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-hydroxy-5-trityloxymethyl-5H-furan-2-one(862546-71-2)
    11. EPA Substance Registry System: 4-hydroxy-5-trityloxymethyl-5H-furan-2-one(862546-71-2)

  • 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: 862546-71-2(Hazardous Substances Data)

862546-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862546-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,5,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 862546-71:
(8*8)+(7*6)+(6*2)+(5*5)+(4*4)+(3*6)+(2*7)+(1*1)=192
192 % 10 = 2
So 862546-71-2 is a valid CAS Registry Number.

862546-71-2Relevant articles and documents

Solution-phase and solid-phase syntheses of enzyme inhibitor RK-682 and antibiotic agglomerins

Schobert, Rainer,Jagusch, Garsten

, p. 6129 - 6132 (2007/10/03)

The enzyme inhibitor RK-682 (5A)-(+)-1 was prepared in solution and on a solid support from (2R)-glycerates in five steps and ca. 40% overall yield. Key steps were a ring-closing tandem addition-Wittig alkenation reaction of the respective protected or im

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