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3-Fluoro-N-n-hexylbenzylaMine, 97% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1042511-87-4 Structure
  • Basic information

    1. Product Name: 3-Fluoro-N-n-hexylbenzylaMine, 97%
    2. Synonyms: 3-Fluoro-N-n-hexylbenzylaMine, 97%
    3. CAS NO:1042511-87-4
    4. Molecular Formula: C13H20FN
    5. Molecular Weight: 209.3030032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1042511-87-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Fluoro-N-n-hexylbenzylaMine, 97%(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Fluoro-N-n-hexylbenzylaMine, 97%(1042511-87-4)
    11. EPA Substance Registry System: 3-Fluoro-N-n-hexylbenzylaMine, 97%(1042511-87-4)
  • 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: 1042511-87-4(Hazardous Substances Data)

1042511-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042511-87-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,5,1 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1042511-87:
(9*1)+(8*0)+(7*4)+(6*2)+(5*5)+(4*1)+(3*1)+(2*8)+(1*7)=104
104 % 10 = 4
So 1042511-87-4 is a valid CAS Registry Number.

1042511-87-4Downstream Products

1042511-87-4Relevant articles and documents

One-pot, chemoselective synthesis of secondary amines from aryl nitriles using a PdPt-Fe3O4nanoparticle catalyst

Byun, Sangmoon,Cho, Ahra,Cho, Jin Hee,Kim, B. Moon

, p. 4201 - 4209 (2020/09/23)

We have developed a new catalytic method for the one-pot, cascade synthesis of unsymmetrical secondary amines via the reductive amination of aryl nitriles with nitroalkanes using a PdPt-Fe3O4 nanoparticle (NP) catalyst. The use of a bimetallic catalyst resulted in enhanced reactivity and selectivity compared to that of either monometallic Pd-Fe3O4 or the Pt-Fe3O4 NP catalyst. Using this bimetallic catalytic system, we were successful in the synthesis of various unsymmetrical secondary amines under mild conditions. However, aryl nitriles containing an electron-donating substituent were rather resistant to the reductive amination, and when hexafluoroisopropanol (HFIP) was used as a co-solvent, the reaction selectivity and yield for unsymmetrical secondary amines increased dramatically. Using the catalyst system, one-pot, gram-scale synthesis of indole was possible from 2-nitrophenylacetonitrile. Due to the magnetic property of the Fe3O4 support, the bimetallic catalyst could easily be recycled using an external magnet at least four times.

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