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methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-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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  • 219313-13-0 Structure
  • Basic information

    1. Product Name: methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside
    2. Synonyms: methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside
    3. CAS NO:219313-13-0
    4. Molecular Formula:
    5. Molecular Weight: 441.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219313-13-0.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-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside(219313-13-0)
    11. EPA Substance Registry System: methyl 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranoside(219313-13-0)
  • 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: 219313-13-0(Hazardous Substances Data)

219313-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219313-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,3,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 219313-13:
(8*2)+(7*1)+(6*9)+(5*3)+(4*1)+(3*3)+(2*1)+(1*3)=110
110 % 10 = 0
So 219313-13-0 is a valid CAS Registry Number.

219313-13-0Downstream Products

219313-13-0Relevant articles and documents

Synthesis and glycosidic coupling reaction of substituted 2,6-dioxabicyco[3.1.1] heptanes: 1,3-anhydro-2-azido-4,6-di-O-benzyl-2-deoxy-β-D-mannopyranose

Yang, Guangbin,Kong, Fanzuo

, p. 77 - 83 (2007/10/03)

The title 1,3-anhydro sugar was synthesized from methyl α-D-glucopyranoside. The key intermediate for the synthesis was 3-O-acetyl-2-azido-4,6-di-O-benzyl-2-deoxy-α-D-mannopyranosyl chloride (11) which was transformed into the target compound by ring closure with potassium tert-butoxide. Copyright (C) 1998 Elsevier Science Ltd.

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