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1-oxacyclohexadec-13-en-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111879-81-3 Structure
  • Basic information

    1. Product Name: 1-oxacyclohexadec-13-en-2-one
    2. Synonyms: oxacyclohexadec-13-en-2-one
    3. CAS NO:111879-81-3
    4. Molecular Formula: C15H26O2
    5. Molecular Weight: 238.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111879-81-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 383.7°C at 760 mmHg
    3. Flash Point: 161.2°C
    4. Appearance: N/A
    5. Density: 0.9g/cm3
    6. Vapor Pressure: 4.31E-06mmHg at 25°C
    7. Refractive Index: 1.445
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-oxacyclohexadec-13-en-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-oxacyclohexadec-13-en-2-one(111879-81-3)
    12. EPA Substance Registry System: 1-oxacyclohexadec-13-en-2-one(111879-81-3)
  • 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: 111879-81-3(Hazardous Substances Data)

111879-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111879-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,7 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111879-81:
(8*1)+(7*1)+(6*1)+(5*8)+(4*7)+(3*9)+(2*8)+(1*1)=133
133 % 10 = 3
So 111879-81-3 is a valid CAS Registry Number.

111879-81-3Downstream Products

111879-81-3Relevant articles and documents

PROCESS FOR PREPARING UNSATURATED LACTONES

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Page/Page column 16-17, (2008/06/13)

The invention relates to a process for preparing saturated or unsaturated lactones. This process involves reacting a bicyclic compound or a monocyclic compound with hydrogen peroxide in the presence of a first acid having a pKa of 3 or less and a first organic solvent, thereby forming a hydroperoxide. The obtained mixture comprising the hydroperoxide is subsequently metered to a mixture of a second organic solvent and a dissociation-enhancing catalyst, optionally comprising a second organic acid. The invention also pertains to a process of preparing the hydroperoxide.

Process for the preparation of 1-hydroperoxy-16-oxabicyclo[10.4.0]hexadecane

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Page/Page column 4; 5, (2008/06/13)

Process for the preparation of 1-hydroperoxy-16-oxabicyclo[10.4.0]hexadecane (DDP-OOH), wherein 13-oxabicyclo[10.4.0]hexadec-1(12)-ene (DDP) and hydrogen peroxide are reacted in a diluent in the presence of a strong acid, the diluent has a pKa value of greater than or equal to 4.5 and the strong acid has a pKa value of less than or equal to 1.5, wherein after the reaction has taken place, the strong acid is neutralized with at least 0.9 molar equivalent of a base.

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