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14233-49-9

2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14233-49-9 Structure

  • Basic information

    1. Product Name: 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol
    2. Synonyms: 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol
    3. CAS NO:14233-49-9
    4. Molecular Formula:
    5. Molecular Weight: 784.992
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14233-49-9.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: 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol(14233-49-9)
    11. EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol(14233-49-9)

  • 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: 14233-49-9(Hazardous Substances Data)

14233-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14233-49-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14233-49:
(7*1)+(6*4)+(5*2)+(4*3)+(3*3)+(2*4)+(1*9)=79
79 % 10 = 9
So 14233-49-9 is a valid CAS Registry Number.

14233-49-9Relevant articles and documents

Chemical synthesis of 1-deoxy-L-fructose and L-sorbose through carbonyl translocation

Wu, Hsin-Pei,Hsu, Nai-Yun,Lu, Tai-Ni,Chang, Che-Chien

, p. 378 - 382 (2015)

Two rare sugars - 1-deoxy-L-fructose and L-sorbose - were synthesized from inexpensive starting materials by a carbonyl translocation method developed in our laboratory. Reduction of a known starting compound gave a 1,5-diol derivative. Selective protecti

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