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CAS

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76626-59-0

C6H9O3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76626-59-0 Structure

  • Basic information

    1. Product Name: C6H9O3
    2. Synonyms: C6H9O3
    3. CAS NO:76626-59-0
    4. Molecular Formula:
    5. Molecular Weight: 129.136
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76626-59-0.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: C6H9O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C6H9O3(76626-59-0)
    11. EPA Substance Registry System: C6H9O3(76626-59-0)

  • 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: 76626-59-0(Hazardous Substances Data)

76626-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76626-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,2 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76626-59:
(7*7)+(6*6)+(5*6)+(4*2)+(3*6)+(2*5)+(1*9)=160
160 % 10 = 0
So 76626-59-0 is a valid CAS Registry Number.

76626-59-0Downstream Products

76626-59-0Relevant articles and documents

Kinetic Applications of Electron Paramagnetic Resonance Spectroscopy. 36. Stereoelectronic Effects in Hydrogen Atom Abstraction from Ethers

Malatesta, V.,Ingold, K. U.

, p. 609 - 614 (1981)

Relative rates of hydrogen atom abstraction by photogenerated tert-butoxyl from a variety of cyclic and acyclic ethers, acetals, and orthoformates have been measured at -60 deg C by an EPR spectroscopic technique.There is a pronounced stereoelectronic effect which produces high rates of abstraction from those C-H bonds adjacent to oxygen which have a relatively small dihedral angle (ca. 30 deg) with respect to the p-type orbital(s) on the oxygen(s).For C-H bonds which have a large dihedral angle (ca. 90 deg) abstraction is very much slower.The barrier to inversion of the 2-methoxy-1,3-dioxolan-2-yl radical is 10 kcal/mol.

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