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1003322-53-9

ethyl 5,5,5-trifluoro-2-oxopentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1003322-53-9 Structure

  • Basic information

    1. Product Name: ethyl 5,5,5-trifluoro-2-oxopentanoate
    2. Synonyms:
    3. CAS NO:1003322-53-9
    4. Molecular Formula:
    5. Molecular Weight: 198.142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1003322-53-9.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: ethyl 5,5,5-trifluoro-2-oxopentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 5,5,5-trifluoro-2-oxopentanoate(1003322-53-9)
    11. EPA Substance Registry System: ethyl 5,5,5-trifluoro-2-oxopentanoate(1003322-53-9)

  • 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: 1003322-53-9(Hazardous Substances Data)

1003322-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1003322-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,3,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1003322-53:
(9*1)+(8*0)+(7*0)+(6*3)+(5*3)+(4*2)+(3*2)+(2*5)+(1*3)=69
69 % 10 = 9
So 1003322-53-9 is a valid CAS Registry Number.

1003322-53-9Downstream Products

1003322-53-9Relevant articles and documents

PYRIDAZINONE COMPOUNDS

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Page/Page column 62, (2008/12/07)

The invention is directed to pyridazinone compounds and pharmaceutical compositions containing such compounds that are useful in treating infections by hepatitis C virus.

Synthesis of new pyridazinone derivatives: 2,6-Disubstituted 5-hydroxy-3(2H)-pyridazinone-4-carboxylic acid ethyl esters

Li, Lian-Sheng,Zhou, Yuefen,Zhao, Jingjing,Dragovich, Peter S.,Stankovic, Nebojsa,Bertolini, Thomas M.,Murphy, Douglas E.,Sun, Zhongxiang,Tran, Chinh V.,Ayida, Benjamin K.,Ruebsam, Frank,Webber, Stephen E.

, p. 3301 - 3308 (2008/09/20)

2,6-Disubstituted 5-hydroxy-3(2H)-pyridazinone-4-carboxylic acid ethyl esters were synthesized from α-keto esters via an efficient three-step sequence including hydrazone formation, acylation with ethyl malonyl chloride, and subsequent Dieckmann cyclizati

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