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1263041-93-5

1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1263041-93-5 Structure

  • Basic information

    1. Product Name: 1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose
    2. Synonyms: 1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose
    3. CAS NO:1263041-93-5
    4. Molecular Formula:
    5. Molecular Weight: 416.449
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1263041-93-5.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: 1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose(1263041-93-5)
    11. EPA Substance Registry System: 1-O-acetyl-2,3-O-isopropylidene-6-O-tosyl-α-D-mannofuranose(1263041-93-5)

  • 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: 1263041-93-5(Hazardous Substances Data)

1263041-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263041-93-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,0,4 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1263041-93:
(9*1)+(8*2)+(7*6)+(6*3)+(5*0)+(4*4)+(3*1)+(2*9)+(1*3)=125
125 % 10 = 5
So 1263041-93-5 is a valid CAS Registry Number.

1263041-93-5Downstream Products

1263041-93-5Relevant articles and documents

Ring-rearrangement metathesis of substituted dihydropyrans and dihydrofurans

Donnard, Morgan,Tschamber, Théophile,Le Nou?n, Didier,Desrat, Sandy,Hinsinger, Karen,Eustache, Jacques

, p. 339 - 357 (2011)

The rearrangement of dihydropyrans and dihydrofurans featuring appending olefins has been studied. The rearranged products bear resemblance with polyunsaturated di- and trisaccharides. Examples of functionalization prior to, or following, rearrangement are provided suggesting that the method should be useful for the synthesis of nonclassical saccharides. This work also illustrates the power of cascade methatetic processes for increasing molecular complexity starting from relatively simple heterocycles. Copyright

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