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CAS

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154902-44-0

(1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154902-44-0 Structure

  • Basic information

    1. Product Name: (1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol
    2. Synonyms: (1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol
    3. CAS NO:154902-44-0
    4. Molecular Formula:
    5. Molecular Weight: 218.175
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154902-44-0.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: (1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol(154902-44-0)
    11. EPA Substance Registry System: (1S,2R)-1-(meta-trifluoromethylphenyl)-2,3-epoxypropan-1-ol(154902-44-0)

  • 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: 154902-44-0(Hazardous Substances Data)

154902-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154902-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,9,0 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154902-44:
(8*1)+(7*5)+(6*4)+(5*9)+(4*0)+(3*2)+(2*4)+(1*4)=130
130 % 10 = 0
So 154902-44-0 is a valid CAS Registry Number.

154902-44-0Relevant articles and documents

Asymmetric syntheses of (S)-Fenfluramine using Sharpless Epoxidation Methods

Goument, Bertrand,Duhamel, Lucette,Mauge, Robert

, p. 171 - 188 (1994)

We describe one synthesis of (S)-fenfluramine and several syntheses of its precursors (R)- and (S)-1-(meta-trifluoromethylphenyl)propan-2-ols.They were obtained from the asymmetric epoxidation of the primary allylic alcohol 5 and from the kinetic resolution with asymmetric epoxidation of teh secondary allylic alcohol 6.

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