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83469-55-0

5-Benzyloxy-2-(13)C-penten is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83469-55-0 Structure

  • Basic information

    1. Product Name: 5-Benzyloxy-2-(13)C-penten
    2. Synonyms: 5-Benzyloxy-2-(13)C-penten
    3. CAS NO:83469-55-0
    4. Molecular Formula:
    5. Molecular Weight: 177.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83469-55-0.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: 5-Benzyloxy-2-(13)C-penten(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Benzyloxy-2-(13)C-penten(83469-55-0)
    11. EPA Substance Registry System: 5-Benzyloxy-2-(13)C-penten(83469-55-0)

  • 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: 83469-55-0(Hazardous Substances Data)

83469-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83469-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83469-55:
(7*8)+(6*3)+(5*4)+(4*6)+(3*9)+(2*5)+(1*5)=160
160 % 10 = 0
So 83469-55-0 is a valid CAS Registry Number.

83469-55-0Relevant articles and documents

MECHANISMUS DER PROTONKATALYSIERTEN GASPHASENDEHYDRATISIERUNG VON FURFURYLALKOHOL

Thies, H.,Wolfschuetz, R.,Frenking, G.,Schmidt, J.,Schwarz, H.

, p. 1647 - 1656 (2007/10/02)

The gas phase proton catalysed water elimination of tetrahydrofurfuryl alcohol (1) gives exclusively the ring-enlarged oxonium-ion 12.There is no experimental indication for the generation of 11 via a -hydrogen migration.From the analysis of appropriately 13C-labelled precursors in combination with collisional activation mass spectrometry the mechanism for the ring-enlargement has been derived, clearly indicating that the oxygen/carbon bond is cleaved.A comparison of the experimental results with computational investigation (ab initio molecular orbital calculations at the 4-31G level) suggests that free tetrahydrofurfuryl cation 7 is not generated in the gas phase solvolysis.The elimination of H2O from the protonated molecule of 1 is a process characterised by anchimeric assistance of the ether oxygen 15.

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