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CAS

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59333-74-3

2-methyl-5-oxohexanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 59333-74-3 Structure

  • Basic information

    1. Product Name: 2-methyl-5-oxohexanal
    2. Synonyms: 2-methyl-5-oxohexanal
    3. CAS NO:59333-74-3
    4. Molecular Formula:
    5. Molecular Weight: 128.171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59333-74-3.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: 2-methyl-5-oxohexanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methyl-5-oxohexanal(59333-74-3)
    11. EPA Substance Registry System: 2-methyl-5-oxohexanal(59333-74-3)

  • 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: 59333-74-3(Hazardous Substances Data)

59333-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59333-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59333-74:
(7*5)+(6*9)+(5*3)+(4*3)+(3*3)+(2*7)+(1*4)=143
143 % 10 = 3
So 59333-74-3 is a valid CAS Registry Number.

59333-74-3Relevant articles and documents

Formation of acetals under rhodium-catalyzed hydroformylation conditions in alcohols

Diebolt, Olivier,Cruzeuil, Clement,Mueller, Christian,Vogt, Dieter

, p. 670 - 677 (2012)

Hydroformylation of terminal alkenes in alcohol solvents leads to the selective formation of the corresponding acetals. The Xantphos ligand gave the best results as well as acetal selectivities higher than 99% and linear/branched ratios of up to 52 were obtained. The scope of the reaction was studied. Acetals were found to be unreactive under hydroaminomethylation conditions. Copyright

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