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  • 85973-62-2 Structure
  • Basic information

    1. Product Name: C34H30O11S
    2. Synonyms:
    3. CAS NO:85973-62-2
    4. Molecular Formula:
    5. Molecular Weight: 646.672
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85973-62-2.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: C34H30O11S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C34H30O11S(85973-62-2)
    11. EPA Substance Registry System: C34H30O11S(85973-62-2)
  • 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: 85973-62-2(Hazardous Substances Data)

85973-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85973-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85973-62:
(7*8)+(6*5)+(5*9)+(4*7)+(3*3)+(2*6)+(1*2)=182
182 % 10 = 2
So 85973-62-2 is a valid CAS Registry Number.

85973-62-2Relevant articles and documents

Anomeric spiroepoxides derived from fructopyranose, and the synthesis of new fructophosphonic acids

Campbell,Heffernan,Lewis

, p. 1237 - 1240 (1991)

The synthesis of D-fructose 1-deoxy 1-phosphonic acid (2) is described utilising the reaction of diethyl trimethylsilyl phosphite with a novel spiro anomeric epoxide, derived from fructose.

DISTRIBUTION OF TAUTOMERS IN ACYLATED KETOSES. AN IMPORTANT FACTOR IN KETOSIDE SYNTHESIS

Kraska, B.,Lichtel, R.

, p. 361 - 364 (2007/10/02)

Formation of tautomers upon acylation of D-fructose and several 1-O-substituted derivatives thereof is studied and appropiate intermediates are used in stereoselective glycoside synthesis.

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