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CAS

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146934-32-9

2-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 146934-32-9 Structure

  • Basic information

    1. Product Name: 2-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride
    2. Synonyms: 2-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride
    3. CAS NO:146934-32-9
    4. Molecular Formula:
    5. Molecular Weight: 388.207
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146934-32-9.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-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride(146934-32-9)
    11. EPA Substance Registry System: 2-Azido-4,6-O-benzylidene-3-O-chloroacetyl-2-deoxy-β-D-glucopyranosyl chloride(146934-32-9)

  • 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: 146934-32-9(Hazardous Substances Data)

146934-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146934-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,9,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146934-32:
(8*1)+(7*4)+(6*6)+(5*9)+(4*3)+(3*4)+(2*3)+(1*2)=149
149 % 10 = 9
So 146934-32-9 is a valid CAS Registry Number.

146934-32-9Downstream Products

146934-32-9Relevant articles and documents

Synthesis of tetrasaccharide building block of the O-specific polysaccharide of Shigella dysenteriae type 1

Pozsgay,Glaudemans,Robbins,Schneerson

, p. 10249 - 10264 (2007/10/02)

A glycosyl trichloroacetimidate derivative (1) of the tetrasaccharide α-D-Galp-(1→3)-α-D-GlcpNAc-(1→3)-α-L-Rhap-(1→3)-α-L-Rhap was synthesized in a highly stereoselective, stepwise manner, using methyl 1-thioglycosides of L-rhamnose, 2-azido-2-deoxy-D-glucose and D-galactose, as major intermediates. The protecting group scenario in compound 1 permits regioselective deblocking at its 'non-reducing end' unit. Therefore 1 is a suitable intermediate for the preparation of extended fragments of the title polysaccharide.

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