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CAS

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73312-30-8

C13H18NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73312-30-8 Structure

  • Basic information

    1. Product Name: C13H18NO2
    2. Synonyms:
    3. CAS NO:73312-30-8
    4. Molecular Formula:
    5. Molecular Weight: 220.291
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73312-30-8.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: C13H18NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H18NO2(73312-30-8)
    11. EPA Substance Registry System: C13H18NO2(73312-30-8)

  • 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: 73312-30-8(Hazardous Substances Data)

73312-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73312-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,1 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73312-30:
(7*7)+(6*3)+(5*3)+(4*1)+(3*2)+(2*3)+(1*0)=98
98 % 10 = 8
So 73312-30-8 is a valid CAS Registry Number.

73312-30-8Downstream Products

73312-30-8Relevant articles and documents

Acyl Nitroxides. Part 4. Estimation of OH Bond Dissociation Energies for N-t-Butylhydroxamic Acids

Jenkins, Terence C.,Perkins, M. John

, p. 717 - 720 (1983)

E.s.r. spectroscopy has been used to determine the equilibrium constants for the hydrogen exchange reactions between N-t-butylhydroxamic acids and the stable piperidine N-oxyl (1); since the O-H bond strength in (1)-H is known, this gives an estimate of the O-H bond strengths in the hydroxamic acids.These are found to be stronger than those in dialkyl nitroxides and increase with increasing electron demand in the acyl group.

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