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CAS

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82469-72-5

3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82469-72-5 Structure

  • Basic information

    1. Product Name: 3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide
    2. Synonyms: 3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide
    3. CAS NO:82469-72-5
    4. Molecular Formula:
    5. Molecular Weight: 672.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82469-72-5.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: 3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide(82469-72-5)
    11. EPA Substance Registry System: 3,4,6-tri-O-benzoyl-2-(benzoyloximino)-2-deoxy-α-D-arabino-hexopyranosyl bromide(82469-72-5)

  • 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: 82469-72-5(Hazardous Substances Data)

82469-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82469-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82469-72:
(7*8)+(6*2)+(5*4)+(4*6)+(3*9)+(2*7)+(1*2)=155
155 % 10 = 5
So 82469-72-5 is a valid CAS Registry Number.

82469-72-5Downstream Products

82469-72-5Relevant articles and documents

Radical-mediated bromination of carbohydrate derivatives: Searching for alternative reaction conditions without carbon tetrachloride

Czifrák, Katalin,Somsák, László

, p. 8849 - 8852 (2002)

KBrO3-Na2S2O4 in CH2Cl2-H2O or PhCF3-H2O biphasic solvent systems was applied to the bromination of several monosaccharide derivatives having capto-datively

Sugar Enolones, XVIII. - Stereocontrolled Functionalization at Proanomeric Centres by Photobromination. - A Novel Efficient Access to Oxo- and Oximinoglycosyl Bromides

Lichtenthaler, Frieder W.,Jarglis, Pan,Hempe, Walter

, p. 1959 - 1972 (2007/10/02)

Suitably O-blocked monosaccharides carrying an electron acceptor group such as an oxo or oximino function next to a proanomeric centre, readily homolyze the corresponding push-pull-substituted C-H bond to give under photobromination conditions the respect

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