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Benzyl-1,4-di-O-benzoyl-β-D-fructopyranosid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124040-53-5 Structure
  • Basic information

    1. Product Name: Benzyl-1,4-di-O-benzoyl-β-D-fructopyranosid
    2. Synonyms:
    3. CAS NO:124040-53-5
    4. Molecular Formula:
    5. Molecular Weight: 478.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124040-53-5.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: Benzyl-1,4-di-O-benzoyl-β-D-fructopyranosid(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzyl-1,4-di-O-benzoyl-β-D-fructopyranosid(124040-53-5)
    11. EPA Substance Registry System: Benzyl-1,4-di-O-benzoyl-β-D-fructopyranosid(124040-53-5)
  • 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: 124040-53-5(Hazardous Substances Data)

124040-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124040-53-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,4 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 124040-53:
(8*1)+(7*2)+(6*4)+(5*0)+(4*4)+(3*0)+(2*5)+(1*3)=75
75 % 10 = 5
So 124040-53-5 is a valid CAS Registry Number.

124040-53-5Downstream Products

124040-53-5Relevant articles and documents

NEUE SYNTHESE UND KRISTALLSTRUKTUR DER LEUCROSE

Thiem, Joachim,Kleeberg, Matthias,Klaska, Karl-Heinz

, p. 65 - 78 (2007/10/02)

Boron trifluoride-catalyzed condensation of 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl fluoride (2) with 3,4-di-O-benzoyl-1,2-O-isopropylidene-β-D-fructopyranose (1) gave preferentially the α-D-(1->5)-linked disaccharide 8.Similarly, glycosylation of benzyl 1,3,4-tri-O-benzoyl-β-D-fructopyranoside (4) with 2 gave preponderantly a disaccharide derivative that, after cleavage of benzoyl as well as benzyl groups, afforded leucrose (5-O-α-D-glucopyranosyl-β-D-fructopyranose; 13).This crystallized in the orthorhombic space group P212121 containing four sugar and four water molecules in the unit cell in two positions in the ratio of 4:1.As expected, both the fructopyranose and the glucopyranose rings adopted the 2C5(D) or 4C1(D) chair conformations, respectively.

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