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467214-80-8

3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 467214-80-8 Structure

  • Basic information

    1. Product Name: 3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone
    2. Synonyms: 3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone
    3. CAS NO:467214-80-8
    4. Molecular Formula:
    5. Molecular Weight: 231.294
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 467214-80-8.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: 3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone(467214-80-8)
    11. EPA Substance Registry System: 3-((R)-2-Hydroxy-1-phenyl-ethylamino)-cyclohex-2-enone(467214-80-8)

  • 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: 467214-80-8(Hazardous Substances Data)

467214-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 467214-80-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,7,2,1 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 467214-80:
(8*4)+(7*6)+(6*7)+(5*2)+(4*1)+(3*4)+(2*8)+(1*0)=158
158 % 10 = 8
So 467214-80-8 is a valid CAS Registry Number.

467214-80-8Relevant articles and documents

Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. Evidence for the first highly stereoselective 6π-electron electrocyclic ring closures of 1-azatrienes

Sklenicka, Heather M.,Hsung, Richard P.,McLaughlin, Michael J.,Wei, Lin-Li,Gerasyuto, Aleksey I.,Brennessel, William B.

, p. 10435 - 10442 (2002)

Evidence is described here to support that a highly stereoselective 6π-electron electrocyclic ring closure of 1-azatrienes is a key step in formal [3 + 3] cycloaddition or annulation reactions of chiral vinylogous amides with α,β-unsaturated iminium salts

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