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  • 1373037-97-8 Structure
  • Basic information

    1. Product Name: C18H22F3NO3
    2. Synonyms: C18H22F3NO3
    3. CAS NO:1373037-97-8
    4. Molecular Formula:
    5. Molecular Weight: 357.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373037-97-8.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: C18H22F3NO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H22F3NO3(1373037-97-8)
    11. EPA Substance Registry System: C18H22F3NO3(1373037-97-8)
  • 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: 1373037-97-8(Hazardous Substances Data)

1373037-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373037-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,0,3 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1373037-97:
(9*1)+(8*3)+(7*7)+(6*3)+(5*0)+(4*3)+(3*7)+(2*9)+(1*7)=158
158 % 10 = 8
So 1373037-97-8 is a valid CAS Registry Number.

1373037-97-8Downstream Products

1373037-97-8Relevant articles and documents

A simple method for asymmetric trifluoromethylation of N-acyl oxazolidinones via Ru-catalyzed radical addition to zirconium enolates

Herrmann, Aaron T.,Smith, Lindsay L.,Zakarian, Armen

, p. 6976 - 6979 (2012/06/15)

A Ru-catalyzed direct thermal trifluoromethylation and perfluoroalkylation of N-acyloxazolidinones has been developed. The reaction is experimentally simple and requires inexpensive reagents while providing good yields of products with good levels of stereocontrol. Preliminary studies have shown notable compatibility with functional groups, aromatics, and certain heteroaromatic substituents. The described method provides a useful alternative for the synthesis of fluorinated materials in an experimentally convenient manner.

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