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148960-96-7

7-Benzyloxy-2,3-dioxo-heptanoic acid diethylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148960-96-7 Structure

  • Basic information

    1. Product Name: 7-Benzyloxy-2,3-dioxo-heptanoic acid diethylamide
    2. Synonyms:
    3. CAS NO:148960-96-7
    4. Molecular Formula:
    5. Molecular Weight: 319.401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148960-96-7.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: 7-Benzyloxy-2,3-dioxo-heptanoic acid diethylamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Benzyloxy-2,3-dioxo-heptanoic acid diethylamide(148960-96-7)
    11. EPA Substance Registry System: 7-Benzyloxy-2,3-dioxo-heptanoic acid diethylamide(148960-96-7)

  • 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: 148960-96-7(Hazardous Substances Data)

148960-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148960-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,9,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148960-96:
(8*1)+(7*4)+(6*8)+(5*9)+(4*6)+(3*0)+(2*9)+(1*6)=177
177 % 10 = 7
So 148960-96-7 is a valid CAS Registry Number.

148960-96-7Downstream Products

148960-96-7Relevant articles and documents

Facile synthesis of the 'tricarbonyl' subunit in the immunosuppressant rapamycin

Pattenden,Tankard,Cherry

, p. 2677 - 2680 (2007/10/02)

A concise synthetic route to the tricarbonyl subunit (3a) in the immunosuppressant rapamycin (2), based on ruthenium-catalysed oxidation of an acetylenic amide precursor (17) is described, viz (17) → (18) → (20).

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