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CAS

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79774-49-5

methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79774-49-5 Structure

  • Basic information

    1. Product Name: methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside
    2. Synonyms: methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside
    3. CAS NO:79774-49-5
    4. Molecular Formula:
    5. Molecular Weight: 327.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79774-49-5.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: methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside(79774-49-5)
    11. EPA Substance Registry System: methyl 4-O-benzoyl-6-bromo-2,3,6-trideoxy-α-D-erythro-hex-2-enopyranoside(79774-49-5)

  • 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: 79774-49-5(Hazardous Substances Data)

79774-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79774-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,7 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79774-49:
(7*7)+(6*9)+(5*7)+(4*7)+(3*4)+(2*4)+(1*9)=195
195 % 10 = 5
So 79774-49-5 is a valid CAS Registry Number.

79774-49-5Relevant articles and documents

AN APPLICATION OF THE PALLADIUM-CATALYZED, ALLYLIC AMINATION OF UNSATURATED SUGARS: A NEW SYNTHESIS OF D-FOROSAMINE

Baer, Hans H.,Hanna, Zaher S.

, p. 43 - 56 (1981)

Methyl 4-O-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside, obtainable from methyl 4,6-O-benzylidene-α-D-glucopyranoside (1), was converted into the 2,3-unsaturated 4-benzoate (3) by application of the triiodoimidazole method.Debenzoylation of 3, followed by

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