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2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 190125-74-7 Structure
  • Basic information

    1. Product Name: 2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide
    2. Synonyms: 2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide
    3. CAS NO:190125-74-7
    4. Molecular Formula: C22H20FNO
    5. Molecular Weight: 333.3987032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 190125-74-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 515.6±50.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.164±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.08±0.70(Predicted)
    10. CAS DataBase Reference: 2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide(190125-74-7)
    12. EPA Substance Registry System: 2-(2-fluoro[1,1'-biphenyl]-4-yl)-N-(4-methylphenyl)propanamide(190125-74-7)
  • 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: 190125-74-7(Hazardous Substances Data)

190125-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190125-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,2 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 190125-74:
(8*1)+(7*9)+(6*0)+(5*1)+(4*2)+(3*5)+(2*7)+(1*4)=117
117 % 10 = 7
So 190125-74-7 is a valid CAS Registry Number.

190125-74-7Downstream Products

190125-74-7Relevant articles and documents

CAL-B-mediated efficient synthesis of a set of valuable amides by direct amidation of phenoxy- and aryl-propionic acids

Benamara, Nourelhouda,Merabet-Khelassi, Mounia,Aribi-Zouioueche, Louisa,Riant, Olivier

, p. 4045 - 4053 (2021/04/21)

An efficient, easy and sustainable amidation of a set of non-activated carboxylic acids with anilines, assisted by CAL-B, as biodegradable catalyst, is reported. The enzymatic amidation reactions are performed on set of nonsteroidal anti-inflammatory drugs (NSAIDs), phenoxypropionic acid and protected-prolines by direct condensation of one equivalent of carboxylic acids and two equivalents of anilines derivatives in heptane after 72?h of reaction at 80?°C. The obtained carboxylic amides are recovered with isolated chemical yields varied between moderate and excellent. Fourteen from them are reported for the first time, and an X-ray crystal is obtained for: N-(4-iodophenyl)-2-(4-isobutylphenyl)propanamide 1d.

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