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1263863-22-4

C12H16FN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1263863-22-4 Structure

  • Basic information

    1. Product Name: C12H16FN
    2. Synonyms:
    3. CAS NO:1263863-22-4
    4. Molecular Formula:
    5. Molecular Weight: 193.264
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1263863-22-4.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: C12H16FN(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H16FN(1263863-22-4)
    11. EPA Substance Registry System: C12H16FN(1263863-22-4)

  • 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: 1263863-22-4(Hazardous Substances Data)

1263863-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263863-22-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,8,6 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1263863-22:
(9*1)+(8*2)+(7*6)+(6*3)+(5*8)+(4*6)+(3*3)+(2*2)+(1*2)=164
164 % 10 = 4
So 1263863-22-4 is a valid CAS Registry Number.

1263863-22-4Downstream Products

1263863-22-4Relevant articles and documents

Microwave accelerated three-component fluoroalkylations: Expeditious routes to fluoropharmaceuticals and PET ligands

Placzek, Michael,Labeaume, Paul,Harris, Luke,Ng, Patrick,Daniels, Mathew,Kallmerten, Amy,Jones, Graham B.

, p. 332 - 335 (2011)

One-pot three-component coupling methods have been developed to allow in situ preparation of fluoroalkylated arenes and hydrocarbon chain analogs. The methods, which are accelerated under microwave irradiation gives access to ω-fluorinated alkyl, alkenyl, and alkynyl substituted arenes from readily available precursors. The methods involve late stage introduction of the fluorine and are well suited to application in the synthesis of 18F labeled PET imaging agents.

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