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CAS

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741672-17-3

2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-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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  • 741672-17-3 Structure

  • Basic information

    1. Product Name: 2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-2-deoxy-β-D-glucopyranose
    2. Synonyms: 2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-2-deoxy-β-D-glucopyranose
    3. CAS NO:741672-17-3
    4. Molecular Formula:
    5. Molecular Weight: 936.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 741672-17-3.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: 2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-2-deoxy-β-D-glucopyranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-2-deoxy-β-D-glucopyranose(741672-17-3)
    11. EPA Substance Registry System: 2-acetamido-1,4,6-tris-O-t-butyldiphenylsilyl-2-deoxy-β-D-glucopyranose(741672-17-3)

  • 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: 741672-17-3(Hazardous Substances Data)

741672-17-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 741672-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,6,7 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 741672-17:
(8*7)+(7*4)+(6*1)+(5*6)+(4*7)+(3*2)+(2*1)+(1*7)=163
163 % 10 = 3
So 741672-17-3 is a valid CAS Registry Number.

741672-17-3Relevant articles and documents

An expeditious route to N-Acetyl-D-galactosamine from N-Acetyl-D- glucosamine based on the selective protection of hydroxy groups

Ito, Naoyuki,Tokuda, Yoshihide,Ohba, Shigeru,Sugai, Takeshi

, p. 1181 - 1186 (2004)

GalNAc (1) was straightforwardly prepared from GlcNAc (2a) in six steps. Selective protection of the hydroxy groups on the C-1, C-3, and C-6 positions at the same time was performed by the treatment of TBDPS chloride (5.5 eq.) in DMF in 70% yield. The nuc

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