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CAS

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866915-59-5

(S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 866915-59-5 Structure

  • Basic information

    1. Product Name: (S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone
    2. Synonyms: (S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone
    3. CAS NO:866915-59-5
    4. Molecular Formula:
    5. Molecular Weight: 260.271
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 866915-59-5.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: (S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone(866915-59-5)
    11. EPA Substance Registry System: (S)-(2-azido-5-fluorophenyl)-(2-vinylpyrrolidin-1-yl)methanone(866915-59-5)

  • 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: 866915-59-5(Hazardous Substances Data)

866915-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866915-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,9,1 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 866915-59:
(8*8)+(7*6)+(6*6)+(5*9)+(4*1)+(3*5)+(2*5)+(1*9)=225
225 % 10 = 5
So 866915-59-5 is a valid CAS Registry Number.

866915-59-5Downstream Products

866915-59-5Relevant articles and documents

Effective synthesis of enantiopure [1,2,3]triazolo[1,5-a]- and pyrazolo[1,5-a]-pyrrolo[2,1-c][1,4]benzodiazepines by diastereoselective intramolecular azide and nitrilimine cycloadditions

Broggini, Gianluigi,De Marchi, Ivan,Martinelli, Michela,Paladino, Giuseppe,Pilati, Tullio,Terraneo, Alberto

, p. 2246 - 2252 (2007/10/03)

The synthesis of new tetracyclic 1,4-benzodiazepinonic systems was performed in enantiopure form by totally diastereoselective intramolecular 1,3-dipolar cycloadditions. The absolute stereochemistry of the products was confirmed by X-ray crystallography a

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