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CAS

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1334287-95-4

(S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1334287-95-4 Structure

  • Basic information

    1. Product Name: (S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline
    2. Synonyms: (S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline
    3. CAS NO:1334287-95-4
    4. Molecular Formula:
    5. Molecular Weight: 360.174
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1334287-95-4.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: (S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline(1334287-95-4)
    11. EPA Substance Registry System: (S)-N-(1-(4-bromophenyl)-2,2,2-trifluoroethyl)-4-methoxyaniline(1334287-95-4)

  • 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: 1334287-95-4(Hazardous Substances Data)

1334287-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1334287-95-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,2,8 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1334287-95:
(9*1)+(8*3)+(7*3)+(6*4)+(5*2)+(4*8)+(3*7)+(2*9)+(1*5)=164
164 % 10 = 4
So 1334287-95-4 is a valid CAS Registry Number.

1334287-95-4Downstream Products

1334287-95-4Relevant articles and documents

Palladium(II)-Catalyzed Enantioselective Synthesis of α-(Trifluoromethyl)arylmethylamines

Johnson, Thomas,Luo, Bo,Lautens, Mark

, p. 4923 - 4930 (2016/07/06)

We describe a method for the synthesis of α-(trifluoromethyl)arylmethylamines that consists of the palladium(II)-catalyzed addition of arylboroxines to imines derived from trifluoroacetaldehyde. Palladium acetate is used as a catalyst with electron-neutral or electron-rich arylboroxines, and it was found that addition of an ammonium or silver salt was crucial to promote the reaction of electron-poor boroxines. With (S)-t-Bu-PyOX as the chiral ligand, this method delivers a variety of α-trifluoromethylated amines in 57-91% yield and with greater than 92% ee in most cases.

Chiral phosphoric acid catalyzed transfer hydrogenation: Facile synthetic access to highly optically active trifluoromethylated amines

Henseler, Alexander,Kato, Masanori,Mori, Keiji,Akiyama, Takahiko

, p. 8180 - 8183 (2011/10/09)

Amines to an end: Highly optically active α-CF3- functionalized amines can be obtained using metal-free reaction conditions. The method involves the transfer hydrogenation of CF3-substituted ketimines catalyzed by 1 and reductive ami

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