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510728-30-0

(S)-3-benzylamino-4-phenyl-1-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 510728-30-0 Structure

  • Basic information

    1. Product Name: (S)-3-benzylamino-4-phenyl-1-butene
    2. Synonyms: (S)-3-benzylamino-4-phenyl-1-butene
    3. CAS NO:510728-30-0
    4. Molecular Formula:
    5. Molecular Weight: 237.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 510728-30-0.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: (S)-3-benzylamino-4-phenyl-1-butene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-benzylamino-4-phenyl-1-butene(510728-30-0)
    11. EPA Substance Registry System: (S)-3-benzylamino-4-phenyl-1-butene(510728-30-0)

  • 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: 510728-30-0(Hazardous Substances Data)

510728-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 510728-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,0,7,2 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 510728-30:
(8*5)+(7*1)+(6*0)+(5*7)+(4*2)+(3*8)+(2*3)+(1*0)=120
120 % 10 = 0
So 510728-30-0 is a valid CAS Registry Number.

510728-30-0Relevant articles and documents

Stereoselective copper-catalyzed intramolecular alkene aminooxygenation: Effects of substrate and ligand structure on selectivity

Paderes, Monissa C.,Chemler, Sherry R.

, p. 3679 - 3684 (2011/09/16)

A new protocol for diastereoselective copper-catalyzed intramolecular alkene aminooxygenation, which provides methyleneoxy-functionalized disubstituted pyrrolidines and five-membered cyclic ureas from the corresponding γ-alkenylsulfonamides and N-allylure

A highly enantioselective allylic amination reaction using a commercially available chiral rhodium catalyst: Resolution of racemic allylic carbonates

Vrieze, Derek C.,Hoge, Garrett S.,Hoerter, Perrine Z.,Van Haitsma, Jared T.,Samas, Brian M.

supporting information; experimental part, p. 3140 - 3142 (2009/12/06)

A novel method for the kinetic resolution of unsymmetrical acyclic allylic carbonates and the concurrent synthesis of enantioenriched secondary amines using a commercially available chiral catalyst is disclosed.

Synthesis of functionalized piperidinones

Humphries, Mark E.,Murphy, James,Phillips, Andrew J.,Abell, Andrew D.

, p. 2432 - 2436 (2007/10/03)

A versatile, stereoselective synthesis of 5-hydroxypiperidinones with substituents at N1, C3, and C6 has been developed. The sequence involves ring-closing metathesis of a diene amide and epoxidation of the resulting alkene, followed by base-mediated elim

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