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CAS

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3225-27-2

C17H24NO5 is a chemical compound with a molecular formula indicating it contains 17 carbon atoms, 24 hydrogen atoms, 1 nitrogen atom, and 5 oxygen atoms. C17H24NO5 likely belongs to a class of organic molecules, possibly a derivative of a phenol or a complex ester, given the presence of a nitrogen atom and multiple oxygen atoms. The specific structure and properties of C17H24NO5 would depend on the arrangement of these atoms and the functional groups present. Without additional information, it's challenging to determine its exact nature, but it could be a pharmaceutical, a natural product, or a synthetic compound used in various industries.

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  • 3225-27-2 Structure

  • Basic information

    1. Product Name: C17H24NO5
    2. Synonyms:
    3. CAS NO:3225-27-2
    4. Molecular Formula:
    5. Molecular Weight: 322.381
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3225-27-2.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: C17H24NO5(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H24NO5(3225-27-2)
    11. EPA Substance Registry System: C17H24NO5(3225-27-2)

  • 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: 3225-27-2(Hazardous Substances Data)

3225-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3225-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3225-27:
(6*3)+(5*2)+(4*2)+(3*5)+(2*2)+(1*7)=62
62 % 10 = 2
So 3225-27-2 is a valid CAS Registry Number.

3225-27-2Downstream Products

3225-27-2Relevant articles and documents

Novel 2,2,6,6-tetramethylpiperidine 1-oxyl-iodobenzene hybrid catalyst for oxidation of primary alcohols to carboxylic acids

Yakura, Takayuki,Ozono, Ayaka

, p. 855 - 859 (2011)

Novel bifunctional hybrid-type catalysts bearing 2,2,6,6- tetramethylpiperidine-1-oxyl (TEMPO) and iodobenzene moieties (1a and 1b) were developed and used for the environmentally benign oxidation of primary alcohols to carboxylic acids. Reaction of primary alcohols 2 with a catalytic amount of 1 in the presence of peracetic acid as a co-oxidant under mild conditions gave the corresponding carboxylic acids 3 in excellent yields.

A time-resolved electron paramagnetic resonance investigation of the spin exchange and chemical interactions of reactive free radicals with isotopically symmetric (14N-X-14N) and isotopically asymmetric ( 14N-X-15

Sartori, Elena,Khudyakov, Igor V.,Lei, Xuegong,Turro, Nicholas J.

, p. 7785 - 7792 (2008/02/09)

Interactions between reactive free radicals (r) with stable mononitroxyl radicals (N) and bisnitroxyl radicals (N-X-N) were studied by time-resolved electron paramagnetic resonance (TR-EPR). Reactive spin-polarized free radicals (r#), with non-

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