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1628200-33-8

C11H8F3NO3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1628200-33-8 Structure

  • Basic information

    1. Product Name: C11H8F3NO3
    2. Synonyms: C11H8F3NO3
    3. CAS NO:1628200-33-8
    4. Molecular Formula:
    5. Molecular Weight: 259.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1628200-33-8.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: C11H8F3NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C11H8F3NO3(1628200-33-8)
    11. EPA Substance Registry System: C11H8F3NO3(1628200-33-8)

  • 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: 1628200-33-8(Hazardous Substances Data)

1628200-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1628200-33-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,8,2,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1628200-33:
(9*1)+(8*6)+(7*2)+(6*8)+(5*2)+(4*0)+(3*0)+(2*3)+(1*3)=138
138 % 10 = 8
So 1628200-33-8 is a valid CAS Registry Number.

1628200-33-8Downstream Products

1628200-33-8Relevant articles and documents

Copper-catalyzed decarboxylative trifluoromethylation of propargyl bromodifluoroacetates

Ambler, Brett R.,Peddi, Santosh,Altman, Ryan A.

, p. 1938 - 1946 (2014)

The development of efficient methods for accessing fluoA rinated functional groups is desirable. Herein, we report a two step method that utilizes catalytic copper for the decarboxylative trifluoromethylation of propargyl bromodifluoroacetates is described. This protocol affords a mixture of propargyl trifluoromethanes and trifluoromethyl allenes. Georg Thieme Verlag Stuttgart New York.

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