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1333149-07-7

C18H30O is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1333149-07-7 Structure

  • Basic information

    1. Product Name: C18H30O
    2. Synonyms: C18H30O
    3. CAS NO:1333149-07-7
    4. Molecular Formula:
    5. Molecular Weight: 262.436
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1333149-07-7.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: C18H30O(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H30O(1333149-07-7)
    11. EPA Substance Registry System: C18H30O(1333149-07-7)

  • 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: 1333149-07-7(Hazardous Substances Data)

1333149-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333149-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,1,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1333149-07:
(9*1)+(8*3)+(7*3)+(6*3)+(5*1)+(4*4)+(3*9)+(2*0)+(1*7)=127
127 % 10 = 7
So 1333149-07-7 is a valid CAS Registry Number.

1333149-07-7Downstream Products

1333149-07-7Relevant articles and documents

Cyanocuprates convert carboxylic acids directly into ketones

Genna, Douglas T.,Posner, Gary H.

, p. 5358 - 5361 (2011)

Carboxylic acids were converted directly in 56-99% yields into methyl, n-butyl, and isopropyl ketones using excess cyanocuprates R2CuLi 3 LiCN. A substrate with a stereocenter α to the carboxylic acid was converted into ketones with very little loss of enantiomeric purity. A variety of functional groups were tolerated including aryl bromides. This direct transformation of a carboxylic acid into ketone with minimal tertiary alcohol formation is proposed to involve a relatively stable copper ketal tetrahedral intermediate.

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