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CAS

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189163-36-8

Acetamide, 2,2,2-trifluoro-N-[2-hydroxy-3-(phenylmethoxy)propyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 189163-36-8 Structure

  • Basic information

    1. Product Name: Acetamide, 2,2,2-trifluoro-N-[2-hydroxy-3-(phenylmethoxy)propyl]-, (R)-
    2. Synonyms:
    3. CAS NO:189163-36-8
    4. Molecular Formula: C12H14F3NO3
    5. Molecular Weight: 277.243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 189163-36-8.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: Acetamide, 2,2,2-trifluoro-N-[2-hydroxy-3-(phenylmethoxy)propyl]-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-[2-hydroxy-3-(phenylmethoxy)propyl]-, (R)-(189163-36-8)
    11. EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-[2-hydroxy-3-(phenylmethoxy)propyl]-, (R)-(189163-36-8)

  • 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: 189163-36-8(Hazardous Substances Data)

189163-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 189163-36-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,1,6 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 189163-36:
(8*1)+(7*8)+(6*9)+(5*1)+(4*6)+(3*3)+(2*3)+(1*6)=168
168 % 10 = 8
So 189163-36-8 is a valid CAS Registry Number.

189163-36-8Relevant articles and documents

Regioselective opening of epoxides to β-amido alcohols under solid-liquid PTC conditions

Albanese, Domenico,Landini, Dario,Penso, Michele

, p. 4787 - 4790 (1997)

A study on the ring opening of a number of epoxides 1 with trifluoroacetamide (2) under solid-liquid phase transfer catalysis (SL-PTC) conditions has been performed. The reaction is completely regioselective affording β-amido alcohols 3 deriving from the attack of the nucleophile to the less substituted carbon atom of the oxirane ring.

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