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CAS

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209523-08-0

(Z)-N,N-dibenzyl-3,3,3-trifluoro-1-phenylprop-1-en-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 209523-08-0 Structure

  • Basic information

    1. Product Name: (Z)-N,N-dibenzyl-3,3,3-trifluoro-1-phenylprop-1-en-2-amine
    2. Synonyms:
    3. CAS NO:209523-08-0
    4. Molecular Formula:
    5. Molecular Weight: 367.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 209523-08-0.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: (Z)-N,N-dibenzyl-3,3,3-trifluoro-1-phenylprop-1-en-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-N,N-dibenzyl-3,3,3-trifluoro-1-phenylprop-1-en-2-amine(209523-08-0)
    11. EPA Substance Registry System: (Z)-N,N-dibenzyl-3,3,3-trifluoro-1-phenylprop-1-en-2-amine(209523-08-0)

  • 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: 209523-08-0(Hazardous Substances Data)

209523-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209523-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,5,2 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 209523-08:
(8*2)+(7*0)+(6*9)+(5*5)+(4*2)+(3*3)+(2*0)+(1*8)=120
120 % 10 = 0
So 209523-08-0 is a valid CAS Registry Number.

209523-08-0Downstream Products

209523-08-0Relevant articles and documents

Palladium-catalyzed amination of 2,3,3-trifluoroallyl esters: Synthesis of trifluoromethylenamines via an intramolecular fluorine shift and CF3 group construction

Isa, Kazuki,Minakawa, Maki,Kawatsura, Motoi

, p. 6761 - 6764 (2015)

The palladium-catalyzed reaction of 2,3,3-trifluoroallyl esters with several types of amines afforded trifluoromethylenamines, which were formed by the addition of a nitrogen nucleophile at the C-2 position and the intramolecular construction of the trifluoromethyl group via the fluorine atom shift from the C-2 to the C-3 position.

Concise stereoselective synthesis of 1-perfluoroalkyl enamines via the addition of N-lithiated amines to enol ethers and their subsequent metalation to form new functionalized enamines

Begue, Jean-Pierre,Bonnet-Delpon, Daniele,Bouvet, Denis,Rock, Michael H.

, p. 1797 - 1800 (1998)

Addition of lithium amides derived from a range of cyclic, sterically demanding, and chiral amines, to trifluoromethyl (Z)-enol ethers 1 and 4, provides stereoselectively the corresponding (Z)-enamines 3a-e and 7 in good yields. This reaction has been ext

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