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benzyl 5-azido-5-deoxy-α-D-mannofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94119-04-7 Structure
  • Basic information

    1. Product Name: benzyl 5-azido-5-deoxy-α-D-mannofuranoside
    2. Synonyms: benzyl 5-azido-5-deoxy-α-D-mannofuranoside
    3. CAS NO:94119-04-7
    4. Molecular Formula:
    5. Molecular Weight: 295.295
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94119-04-7.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: benzyl 5-azido-5-deoxy-α-D-mannofuranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzyl 5-azido-5-deoxy-α-D-mannofuranoside(94119-04-7)
    11. EPA Substance Registry System: benzyl 5-azido-5-deoxy-α-D-mannofuranoside(94119-04-7)
  • 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: 94119-04-7(Hazardous Substances Data)

94119-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94119-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 94119-04:
(7*9)+(6*4)+(5*1)+(4*1)+(3*9)+(2*0)+(1*4)=127
127 % 10 = 7
So 94119-04-7 is a valid CAS Registry Number.

94119-04-7Downstream Products

94119-04-7Relevant articles and documents

SYNTHESES OF 1,5-DIDEOXY-1,5-IMINO-D-MANNITOL FROM D-MANNOSE AND D-GLUCOSE

Fleet, G. W. J.,Gough, M. J.,Shing, T. K. M.

, p. 4029 - 4032 (2007/10/02)

Unambigous enantiospecific syntheses of 1,5-dideoxy-1,5-imino-D-mannitol (LU1, 1-deoxy-mannojirimycin) are reported (i) from D-mannose via hydrogenation of a 5-azido-5-deoxy mannose, and (ii) from D-glucose, in which the key step involves nucleophilic substitution of a trifluoromethanesulphonyl group from C-2 of D-glucose.

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