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162635-57-6

3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162635-57-6 Structure

  • Basic information

    1. Product Name: 3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol
    2. Synonyms: 3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol
    3. CAS NO:162635-57-6
    4. Molecular Formula:
    5. Molecular Weight: 686.847
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162635-57-6.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: 3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol(162635-57-6)
    11. EPA Substance Registry System: 3-O-p-tolylsulfonyl-2-O-(2-p-tolylsulfonyloxyethyl)-1-O-(triphenylmethyl)glycerol(162635-57-6)

  • 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: 162635-57-6(Hazardous Substances Data)

162635-57-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162635-57-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,6,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162635-57:
(8*1)+(7*6)+(6*2)+(5*6)+(4*3)+(3*5)+(2*5)+(1*7)=136
136 % 10 = 6
So 162635-57-6 is a valid CAS Registry Number.

162635-57-6Downstream Products

162635-57-6Relevant articles and documents

A new route to some enantiomerically pure substituted morpholines from D-ribono- and D-gulono-1,4-lactones

Bennis, Khalil,Calinaud, Pierre,Gelas, Jacques,Ghobsi, Mebrouk

, p. 33 - 44 (2007/10/02)

D-Ribono-1,4-lactone, after acetalation, tritylation, and reduction, leads to a cyclization compound which gave with tosyl chloride 1,4-anhydro-2,3-O-isopropylidene-5-O-trityl-D-ribitol.The latter was transformed (acid hydrolysis, periodate oxidation, reduction, tritylation, and tosylation) into a ditosylated derivative 16, which was cyclized into morpholines by the action of primary amines.Acid hydrolysis, followed by acetylation, gives the (2S)-acetoxymethyl-4-isopropyltetrahydro-1,4-oxazine (21).A similar sequence has been applied to D-gulonolactone to give access to oxazines 33, 34, and 35. Keywords: Synthesis; D-Ribono-1,4-lactone; D-Gulono-1,4-lactone; Morpholine derivatives

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