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64526-69-8

isopropyl β-D-xylofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64526-69-8 Structure

  • Basic information

    1. Product Name: isopropyl β-D-xylofuranoside
    2. Synonyms:
    3. CAS NO:64526-69-8
    4. Molecular Formula:
    5. Molecular Weight: 192.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64526-69-8.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: isopropyl β-D-xylofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: isopropyl β-D-xylofuranoside(64526-69-8)
    11. EPA Substance Registry System: isopropyl β-D-xylofuranoside(64526-69-8)

  • 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: 64526-69-8(Hazardous Substances Data)

64526-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64526-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,2 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64526-69:
(7*6)+(6*4)+(5*5)+(4*2)+(3*6)+(2*6)+(1*9)=138
138 % 10 = 8
So 64526-69-8 is a valid CAS Registry Number.

64526-69-8Downstream Products

64526-69-8Relevant articles and documents

Direct glycosylation of unprotected and unactivated carbohydrates under mild conditions

Pfaffe, Matthias,Mahrwald, Rainer

, p. 792 - 795 (2012)

Ligand exchange acetalization of acetals in the presence of catalytic amounts of mandelic acid and titanium tert-butoxide is reported. This transformation is successfully extended to glycosylation of unprotected and unactivated pentoses. Even unreactive pentoses such as d-arabinose or d-lyxose can be transformed by this new methodology into corresponding isopropyl glycosides.

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