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CAS

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1256814-98-8

4,6-di-O-acetyl-2-azido-3-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1256814-98-8 Structure

  • Basic information

    1. Product Name: 4,6-di-O-acetyl-2-azido-3-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranoside
    2. Synonyms:
    3. CAS NO:1256814-98-8
    4. Molecular Formula:
    5. Molecular Weight: 493.632
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1256814-98-8.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: 4,6-di-O-acetyl-2-azido-3-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,6-di-O-acetyl-2-azido-3-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranoside(1256814-98-8)
    11. EPA Substance Registry System: 4,6-di-O-acetyl-2-azido-3-O-benzyl-1-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranoside(1256814-98-8)

  • 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: 1256814-98-8(Hazardous Substances Data)

1256814-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256814-98-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,8,1 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1256814-98:
(9*1)+(8*2)+(7*5)+(6*6)+(5*8)+(4*1)+(3*4)+(2*9)+(1*8)=178
178 % 10 = 8
So 1256814-98-8 is a valid CAS Registry Number.

1256814-98-8Downstream Products

1256814-98-8Relevant articles and documents

Mannosazide methyl uronate donors. Glycosylating properties and use in the construction of β-ManNAcA-containing oligosaccharides

Walvoort, Marthe T. C.,Lodder, Gerrit,Overkleeft, Herman S.,Codee, Jeroen D. C.,Van Der Marel, Gijsbert A.

, p. 7990 - 8002 (2010)

Mannosazide methyl uronate donors equipped with a variety of anomeric leaving groups (β- and α-S-phenyl, β- and α-N- phenyltrifluoroacetimidates, hydroxyl, β-sulfoxide, and (Rs)- and (Ss)-α-sulfoxides) were subjected to activating co

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