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phenyl 3-O-acetyl-6-deoxy-1-thio-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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  • 1432492-20-0 Structure
  • Basic information

    1. Product Name: phenyl 3-O-acetyl-6-deoxy-1-thio-β-D-mannopyranoside
    2. Synonyms: phenyl 3-O-acetyl-6-deoxy-1-thio-β-D-mannopyranoside
    3. CAS NO:1432492-20-0
    4. Molecular Formula:
    5. Molecular Weight: 298.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1432492-20-0.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: phenyl 3-O-acetyl-6-deoxy-1-thio-β-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 3-O-acetyl-6-deoxy-1-thio-β-D-mannopyranoside(1432492-20-0)
    11. EPA Substance Registry System: phenyl 3-O-acetyl-6-deoxy-1-thio-β-D-mannopyranoside(1432492-20-0)
  • 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: 1432492-20-0(Hazardous Substances Data)

1432492-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1432492-20-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,4,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1432492-20:
(9*1)+(8*4)+(7*3)+(6*2)+(5*4)+(4*9)+(3*2)+(2*2)+(1*0)=140
140 % 10 = 0
So 1432492-20-0 is a valid CAS Registry Number.

1432492-20-0Relevant articles and documents

Expeditious synthesis of bacterial, rare sugar building blocks to access the prokaryotic glycome

Emmadi, Madhu,Kulkarni, Suvarn S.

supporting information, p. 3098 - 3102 (2013/06/04)

Bacteria have unusual glycans which are not accessible by isolation. Herein, we describe a general and divergent strategy for the synthesis of the rare, bacterial deoxy amino hexopyranoside building blocks from d-mannose. The methodology is applied to the first total synthesis of the l-serine linked trisaccharide of Neisseria meningitidis. The Royal Society of Chemistry 2013.

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