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115220-40-1

1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115220-40-1 Structure

  • Basic information

    1. Product Name: 1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose
    2. Synonyms: 1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose
    3. CAS NO:115220-40-1
    4. Molecular Formula:
    5. Molecular Weight: 425.56
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115220-40-1.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: 1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose(115220-40-1)
    11. EPA Substance Registry System: 1,6-anhydro-2-azido-4-O-tertbutyldiphenylsilyl-2-deoxy-β-D-glucopyranose(115220-40-1)

  • 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: 115220-40-1(Hazardous Substances Data)

115220-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115220-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115220-40:
(8*1)+(7*1)+(6*5)+(5*2)+(4*2)+(3*0)+(2*4)+(1*0)=71
71 % 10 = 1
So 115220-40-1 is a valid CAS Registry Number.

115220-40-1Relevant articles and documents

A modular strategy toward the synthesis of heparin-like oligosaccharides using monomeric building blocks in a sequential glycosylation strategy

Codee, Jeroen D. C.,Stubba, Bas,Schiattarella, Marialuisa,Overkleeft, Herman S.,Van Boeckel, Constant A. A.,Van Boom, Jacques H.,Van Der Marel, Gijsbert A.

, p. 3767 - 3773 (2005)

A novel flexible assembly strategy is described for the modular synthesis of heparin and heparan sulfates. The reported strategy uses monomeric building bocks to construct the oligosaccharide chain to attain a maximum degree of flexibility. In the assembly, 1-hydroxyl glucosazido- and 1-thio uronic acid donors are combined in a sequential glycosylation protocol using sulfonium triflate activator systems. The key 1-thio uronic acids were obtained in an efficient manner from diacetone glucose employing a chemo- and regioselective oxidation of partially protected glucose and idose thioglycosides.

NOVEL ANTI-INFLAMMATORY PRO-DRUGS

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Page/Page column 19, (2009/01/24)

The present invention relates to compounds according to formula (I): wherein R is selected from the group consisting of anti-inflammatory agents and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising compounds of formula (I) and the use of these pharmaceutical compositions for the treatment or prophylaxis of chronic inflammatory diseases, in particular those that are caused by chronically activated macrophages. The chronic inflammatory disease is in particular atherosclerosis, (rheumatoid) arthritis, an (auto)immune disease or sarcoidosis.

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