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CAS

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364049-15-0

(-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 364049-15-0 Structure

  • Basic information

    1. Product Name: (-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide
    2. Synonyms: (-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide
    3. CAS NO:364049-15-0
    4. Molecular Formula:
    5. Molecular Weight: 393.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 364049-15-0.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: (-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide(364049-15-0)
    11. EPA Substance Registry System: (-)-(2S,SS)-3,3,3-trifluoro-N-(p-methoxyphenyl)-2-aminopropyl-1-(1-naphtyl)sulfoxide(364049-15-0)

  • 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: 364049-15-0(Hazardous Substances Data)

364049-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 364049-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,4,0,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 364049-15:
(8*3)+(7*6)+(6*4)+(5*0)+(4*4)+(3*9)+(2*1)+(1*5)=140
140 % 10 = 0
So 364049-15-0 is a valid CAS Registry Number.

364049-15-0Relevant articles and documents

Enantioselective synthesis of fluorinated α-amino acids and derivatives in combination with ring-closing metathesis: Intramolecular π-stacking interactions as a source of stereocontrol

Fustero, Santos,Volonterio, Alessandro,Zanda, Matteo,Navarro, Antonio,Pina, Belen,Soler, Juan Garcia,Bartolome, Ana,Asensio, Amparo,Simon, Antonio,Bravo, Pierfrancesco,Fronza, Giovanni

, p. 2621 - 2624 (2007/10/03)

(Equation presented) Hydride reduction of C=N bonds stereocontrolled by intramolecular π-stacking interactions of 1-naphthylsulfinyl and N-aryl groups, nonoxidative Pummerer rearrangement, and ring-closing metathesis are efficiently combined in a highly s

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