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(4R,5R)-5-hydroxy-6-(p-toluenesulfonyloxy)-4-hexanolide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 161807-84-7 Structure
  • Basic information

    1. Product Name: (4R,5R)-5-hydroxy-6-(p-toluenesulfonyloxy)-4-hexanolide
    2. Synonyms:
    3. CAS NO:161807-84-7
    4. Molecular Formula:
    5. Molecular Weight: 300.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161807-84-7.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: (4R,5R)-5-hydroxy-6-(p-toluenesulfonyloxy)-4-hexanolide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R,5R)-5-hydroxy-6-(p-toluenesulfonyloxy)-4-hexanolide(161807-84-7)
    11. EPA Substance Registry System: (4R,5R)-5-hydroxy-6-(p-toluenesulfonyloxy)-4-hexanolide(161807-84-7)
  • 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: 161807-84-7(Hazardous Substances Data)

161807-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161807-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,8,0 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161807-84:
(8*1)+(7*6)+(6*1)+(5*8)+(4*0)+(3*7)+(2*8)+(1*4)=137
137 % 10 = 7
So 161807-84-7 is a valid CAS Registry Number.

161807-84-7Downstream Products

161807-84-7Relevant articles and documents

Enantiopure hydroxylactones from L-ascorbic and D-isoascorbic acids. Part I. Synthesis of (-)-muricatacin

Saniere,Charvet,Le Merrer,Depezay

, p. 1653 - 1662 (1995)

From D-isoascorbic acid, via a formal bis-epoxide equivalent with a C-2 axis of symmetry, two possible syntheses of the (-)-Muricatacin are described.

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