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1395349-03-7

(-)-2-[1-(2-hydroxy-1R-phenylethyl)-5-(2-oxo-2-phenylethyl)pyrrolidin-2-yl]acetophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1395349-03-7 Structure

  • Basic information

    1. Product Name: (-)-2-[1-(2-hydroxy-1R-phenylethyl)-5-(2-oxo-2-phenylethyl)pyrrolidin-2-yl]acetophenone
    2. Synonyms:
    3. CAS NO:1395349-03-7
    4. Molecular Formula:
    5. Molecular Weight: 427.543
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1395349-03-7.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: (-)-2-[1-(2-hydroxy-1R-phenylethyl)-5-(2-oxo-2-phenylethyl)pyrrolidin-2-yl]acetophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-2-[1-(2-hydroxy-1R-phenylethyl)-5-(2-oxo-2-phenylethyl)pyrrolidin-2-yl]acetophenone(1395349-03-7)
    11. EPA Substance Registry System: (-)-2-[1-(2-hydroxy-1R-phenylethyl)-5-(2-oxo-2-phenylethyl)pyrrolidin-2-yl]acetophenone(1395349-03-7)

  • 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: 1395349-03-7(Hazardous Substances Data)

1395349-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395349-03-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,3,4 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1395349-03:
(9*1)+(8*3)+(7*9)+(6*5)+(5*3)+(4*4)+(3*9)+(2*0)+(1*3)=187
187 % 10 = 7
So 1395349-03-7 is a valid CAS Registry Number.

1395349-03-7Downstream Products

1395349-03-7Relevant articles and documents

Solvent-free double aza-Michael under ultrasound irradiation: Diastereoselective sequential one-pot synthesis of pyrrolidine Lobelia alkaloids analogues

Amara, Zacharias,Drège, Emmanuelle,Troufflard, Claire,Retailleau, Pascal,Joseph, Delphine

, p. 7148 - 7157 (2012)

Novel 2,5-meso-pyrrolidines have been straightforwardly synthesized from readily available symmetrical double Michael acceptors. The key step rested on an aza-Michael addition of primary alkylamines to bis-enones. Competitive Rauhut-Currier and aza-Michael reactions have been highlighted in protic solvent. Ultrasound activation associated with solvent-free conditions led to the expected pyrrolidines in quantitative yields and excellent stereoselectivities. The optimized conditions have been extended to the sonochemical synthesis of pyrrolidine Lobelia alkaloids analogues in short sequences.

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