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1061566-71-9

methyl 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1061566-71-9 Structure

  • Basic information

    1. Product Name: methyl 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside
    2. Synonyms: methyl 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside
    3. CAS NO:1061566-71-9
    4. Molecular Formula:
    5. Molecular Weight: 438.499
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1061566-71-9.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 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside(1061566-71-9)
    11. EPA Substance Registry System: methyl 3-O-benzyl-2-O-tosyl-α-D-glucopyranoside(1061566-71-9)

  • 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: 1061566-71-9(Hazardous Substances Data)

1061566-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1061566-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,1,5,6 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1061566-71:
(9*1)+(8*0)+(7*6)+(6*1)+(5*5)+(4*6)+(3*6)+(2*7)+(1*1)=139
139 % 10 = 9
So 1061566-71-9 is a valid CAS Registry Number.

1061566-71-9Relevant articles and documents

A convenient synthesis of orthogonally protected 2-deoxystreptamine (2-DOS) as an aminocyclitol scaffold for the development of novel aminoglycoside antibiotic derivatives against bacterial resistance

Bauder, Claude

, p. 2952 - 2960 (2008)

The development of new aminoglycoside analogues to reduce the emergence of bacterial resistance has become a topic of high interest. We describe here a rapid and facile access to orthogonally protected 2-deoxystreptamine (2-DOS), a meso-diaminocyclitol known to be a pivotal component of most active aminoglycosides. Our synthetic approach started from highly protected methyl α-d-glucopyranoside which in turn was converted by a Ferrier rearrangement into an enantiopure polyfunctionalized cyclohexane ring. Finally, two different N-protected groups were successively introduced. The first one was inserted as an oximino benzylether followed by a diastereofacial hydride reduction, working with Me4NBH(OAc)3 only in TFA at low temperature rather than in AcOH as usual. The second group was introduced by displacement of a hydroxyl group through a Mitsunobu reaction using a DPPA-DIAD-Ph3P system for azide transfer. The Royal Society of Chemistry.

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