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6-deoxy-3-C-methyl-2,3,4-tri-O-methylhexopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20735-41-5 Structure
  • Basic information

    1. Product Name: 6-deoxy-3-C-methyl-2,3,4-tri-O-methylhexopyranose
    2. Synonyms:
    3. CAS NO:20735-41-5
    4. Molecular Formula: C10H20O5
    5. Molecular Weight: 220.2628
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20735-41-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 284.5°C at 760 mmHg
    3. Flash Point: 125.9°C
    4. Appearance: N/A
    5. Density: 1.09g/cm3
    6. Vapor Pressure: 0.000341mmHg at 25°C
    7. Refractive Index: 1.457
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 6-deoxy-3-C-methyl-2,3,4-tri-O-methylhexopyranose(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-deoxy-3-C-methyl-2,3,4-tri-O-methylhexopyranose(20735-41-5)
    12. EPA Substance Registry System: 6-deoxy-3-C-methyl-2,3,4-tri-O-methylhexopyranose(20735-41-5)
  • 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: 20735-41-5(Hazardous Substances Data)

20735-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20735-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20735-41:
(7*2)+(6*0)+(5*7)+(4*3)+(3*5)+(2*4)+(1*1)=85
85 % 10 = 5
So 20735-41-5 is a valid CAS Registry Number.

20735-41-5Downstream Products

20735-41-5Relevant articles and documents

SYNTHESIS OF L-NOGALOSE AND ITS ENANTIOMER

Hong, Namgi,Funabashi, Masuo,Yoshimura, Juji

, p. 21 - 28 (2007/10/02)

L-Nogalose (6-deoxy-3-C-methyl-2,3,4-tri-O-methyl-L-mannopyranose) and its enantiomer were synthesized via (a) introduction of the C-methyl branch by successive epoxidation and reduction of methyl 3,6-dideoxy-2,4-di-O-methyl-3-C-methylene-α-L-arabino-hexopyranoside, and (b) deoxygenation at C-6 of methyl 4,6-O-benzylidene-3-C-methyl-2-O-methyl-α-D-mannopyranoside, and O-methylation of the product.

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