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144522-54-3

1,4-anhydro-2,3,5,6-tetra-O-toluene-p-sulphonyl-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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  • 144522-54-3 Structure

  • Basic information

    1. Product Name: 1,4-anhydro-2,3,5,6-tetra-O-toluene-p-sulphonyl-D-glucitol
    2. Synonyms:
    3. CAS NO:144522-54-3
    4. Molecular Formula:
    5. Molecular Weight: 780.916
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144522-54-3.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: 1,4-anhydro-2,3,5,6-tetra-O-toluene-p-sulphonyl-D-glucitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-anhydro-2,3,5,6-tetra-O-toluene-p-sulphonyl-D-glucitol(144522-54-3)
    11. EPA Substance Registry System: 1,4-anhydro-2,3,5,6-tetra-O-toluene-p-sulphonyl-D-glucitol(144522-54-3)

  • 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: 144522-54-3(Hazardous Substances Data)

144522-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144522-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,2 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 144522-54:
(8*1)+(7*4)+(6*4)+(5*5)+(4*2)+(3*2)+(2*5)+(1*4)=113
113 % 10 = 3
So 144522-54-3 is a valid CAS Registry Number.

144522-54-3Downstream Products

144522-54-3Relevant articles and documents

Some 3,5-acetal derivatives of D-glucitol

Al-Kadir, A. Jabbar,Baggett, Neil,Webber, John M.

, p. 249 - 258 (2007/10/02)

Ethylidenation of 1,6-di-O-benzoyl-2,4-O-benzylidene-D-glucitol gave the 3,5-O-ethylidene derivative in poor yield, whereas reaction with 2,2-dimethoxypropane gave the 3,5-O-isopropylidene derivative in good yield.Removal of the benzoyl and benzylidene gr

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