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119530-16-4

(E)-1-Furan-2-yl-3-phenyl-allylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119530-16-4 Structure

  • Basic information

    1. Product Name: (E)-1-Furan-2-yl-3-phenyl-allylamine
    2. Synonyms:
    3. CAS NO:119530-16-4
    4. Molecular Formula:
    5. Molecular Weight: 199.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119530-16-4.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: (E)-1-Furan-2-yl-3-phenyl-allylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-Furan-2-yl-3-phenyl-allylamine(119530-16-4)
    11. EPA Substance Registry System: (E)-1-Furan-2-yl-3-phenyl-allylamine(119530-16-4)

  • 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: 119530-16-4(Hazardous Substances Data)

119530-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119530-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,5,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119530-16:
(8*1)+(7*1)+(6*9)+(5*5)+(4*3)+(3*0)+(2*1)+(1*6)=114
114 % 10 = 4
So 119530-16-4 is a valid CAS Registry Number.

119530-16-4Downstream Products

119530-16-4Relevant articles and documents

Zirconocene Complexes of Imines: General Synthesis, Structure, Reactivity, and in Situ Generation To Prepare Geometrically Pure Allylic Amines

Buchwald, Stephen L.,Watson, Brett T.,Wannamaker, M. Woods,Dewan, John C.

, p. 4486 - 4494 (1989)

A general method for the preparation of zirconocene complexes of imines has been developed.The X-ray crystal structure of the (trimethylsilyl)benzaldimine complex 2b shows that these complexes should be viewed as metallaaziridenes due to significant ?-donation from the zirconium center to the ?* orbitals of the coordinated imine.These complexes undergo a number of chemo-, regio-, and diastereoselective coupling reactions with unsaturated organic compounds to cleanly form metallacyclic compounds.In situ generation of the complexes followed by coupling with alkynes and hydrolysis affords a general route to geometrically pure allylic amines.

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