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CAS

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1093661-08-5

phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-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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  • 1093661-08-5 Structure

  • Basic information

    1. Product Name: phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside
    2. Synonyms: phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside
    3. CAS NO:1093661-08-5
    4. Molecular Formula:
    5. Molecular Weight: 493.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1093661-08-5.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: phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside(1093661-08-5)
    11. EPA Substance Registry System: phenylsulfinyl 3,4,6-tri-O-acetyl-2-bromo-2-deoxy-α-D-mannopyranoside(1093661-08-5)

  • 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: 1093661-08-5(Hazardous Substances Data)

1093661-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1093661-08-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,6,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1093661-08:
(9*1)+(8*0)+(7*9)+(6*3)+(5*6)+(4*6)+(3*1)+(2*0)+(1*8)=155
155 % 10 = 5
So 1093661-08-5 is a valid CAS Registry Number.

1093661-08-5Relevant articles and documents

Addition reactions of benzenesulfinic acid with glycals and 1,2-dibromosugars

Basava, Vikram,Flores, Broc,Giovine, Matthew,Licisyn, Thomas,Walck, Katelyn,Boyko, Walter,Giuliano, Robert

, p. 389 - 400 (2008)

The addition of benzenesulfinic acid to glycals was investigated under various conditions, and optimized yields of the glycosyl phenylsulfone products were obtained in the presence of tin tetrachloride as a catalyst. Double bond shift (Ferrier rearrangement) occurred in all cases except amicetal, which lacks a substituent at the allylic carbon. Glycosylation of benzenesulfinic acid with 1,2-dibromides was carried out using silver triflate as the promoter, and gave sulfinate esters as products by reaction at oxygen rather than at sulfur. The sulfinate esters were obtained as mixtures of stereoisomers at the stereogenic sulfur atom. Trapping of the sulfinates with carboxylate nucleophiles was observed during attempted oxidation with MCPBA. Copyright Taylor & Francis Group, LLC.

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