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CAS

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89064-70-0

2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89064-70-0 Structure

  • Basic information

    1. Product Name: 2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose
    2. Synonyms: 2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose
    3. CAS NO:89064-70-0
    4. Molecular Formula:
    5. Molecular Weight: 569.654
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89064-70-0.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: 2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose(89064-70-0)
    11. EPA Substance Registry System: 2,3,4,6-Tetra-O-benzyl-1-desoxy-1-nitro-D-glucopyranose(89064-70-0)

  • 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: 89064-70-0(Hazardous Substances Data)

89064-70-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89064-70-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89064-70:
(7*8)+(6*9)+(5*0)+(4*6)+(3*4)+(2*7)+(1*0)=160
160 % 10 = 0
So 89064-70-0 is a valid CAS Registry Number.

89064-70-0Downstream Products

89064-70-0Relevant articles and documents

Desoxy-nitrozucker. Herstellung geschuetzter 1-Deoxy-1-nitroaldosen

Aebischer, Bernard,Vasella, Andrea,Weber, Hans-Peter

, p. 621 - 634 (1982)

The direct oxidation of the oxime 1 with t-butyl hydroperoxide and vanadyl acetylacetonate yielding the nitro derivative 2 (54percent, Scheme 1) could not be applied to other oximes.Diastereoselective bromination of the aldonolactone oxims 7 and 10-12 acc

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