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56078-11-6

Methyl-10-keto-11-hydroxyundecanoat is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56078-11-6 Structure

  • Basic information

    1. Product Name: Methyl-10-keto-11-hydroxyundecanoat
    2. Synonyms: Methyl-10-keto-11-hydroxyundecanoat
    3. CAS NO:56078-11-6
    4. Molecular Formula:
    5. Molecular Weight: 230.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56078-11-6.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: Methyl-10-keto-11-hydroxyundecanoat(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl-10-keto-11-hydroxyundecanoat(56078-11-6)
    11. EPA Substance Registry System: Methyl-10-keto-11-hydroxyundecanoat(56078-11-6)

  • 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: 56078-11-6(Hazardous Substances Data)

56078-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56078-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,7 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56078-11:
(7*5)+(6*6)+(5*0)+(4*7)+(3*8)+(2*1)+(1*1)=126
126 % 10 = 6
So 56078-11-6 is a valid CAS Registry Number.

56078-11-6Upstream product

56078-11-6Downstream Products

56078-11-6Relevant articles and documents

Ruthenium-catalyzed oxidative cleavage of olefins to aldehydes

Yang,Zhang

, p. 4814 - 4818 (2001)

Three oxidation protocols have been developed to cleave olefins to carbonyl compounds with ruthenium trichloride as catalyst (3.5 mol %). These methods convert olefins that are not fully substituted to aldehydes rather than carboxylic acids. While aryl olefins were cleaved to aromatic aldehydes in excellent yields by using the system of RuCl3-Oxone-NaHCO3 in CH3CN-H2O (1.5:1), aliphatic olefins were converted into alkyl aldehydes with RuCl3-NaIO4 in 1,2-dichloroethane-H2O (1:1) in good to excellent yields. It is noteworthy that terminal aliphatic olefins were cleaved to the corresponding aldehydes in excellent yields by using RuCl3-NaIO4 in CH3CN-H2O (6:1).

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