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1428238-29-2

methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-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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  • methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

    Cas No: 1428238-29-2

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  • methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside

    Cas No: 1428238-29-2

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  • 1428238-29-2 Structure

  • Basic information

    1. Product Name: methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside
    2. Synonyms: methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside
    3. CAS NO:1428238-29-2
    4. Molecular Formula:
    5. Molecular Weight: 1599.78
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428238-29-2.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 (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside(1428238-29-2)
    11. EPA Substance Registry System: methyl (6-O-benzyl-2,3,4-tri-O-methyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-β-D-glucopyranosyluronate)-(1→/4)-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1→4)-(methyl 3-O-methyl-α-L-idopyranosyluronate)-(1→/4)-2,3,6-tri-O-benzyl-α-D-glucopyranoside(1428238-29-2)

  • 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: 1428238-29-2(Hazardous Substances Data)

1428238-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428238-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,2,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1428238-29:
(9*1)+(8*4)+(7*2)+(6*8)+(5*2)+(4*3)+(3*8)+(2*2)+(1*9)=162
162 % 10 = 2
So 1428238-29-2 is a valid CAS Registry Number.

1428238-29-2Relevant articles and documents

Novel syntheses of Idraparinux, the anticoagulant pentasaccharide with indirect selective factor Xa inhibitory activity

Herczeg, Mihály,Mez, Erika,Lázár, László,Fekete, Anikó,K?vér, Katalin E.,Antus, Sándor,Borbás, Anikó

, p. 3149 - 3158 (2013/05/09)

Idraparinux, the fully O-sulfated, O-methylated, heparin-related pentasaccharide possessing selective factor Xa inhibitory activity, was prepared by two novel synthetic pathways. Each route was based on a 2+3 block synthesis utilizing the same l-iduronic acid-containing trisaccharide acceptor, which was glycosylated with either a glucuronide disaccharide donor or its non-oxidized precursor. The latter route, involving the oxidation of the glucose unit into d-glucuronic acid at a pentasaccharide level proved to be much more efficient, providing the target pentasaccharide in a reasonable overall yield.

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