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1423027-28-4

(S)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1423027-28-4 Structure

  • Basic information

    1. Product Name: (S)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one
    2. Synonyms: (S)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one
    3. CAS NO:1423027-28-4
    4. Molecular Formula:
    5. Molecular Weight: 283.345
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1423027-28-4.mol
    9. Article Data: 1

  • 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)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one(1423027-28-4)
    11. EPA Substance Registry System: (S)-1-benzyl-4-(4-fluorophenyl)piperidin-3-one(1423027-28-4)

  • 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: 1423027-28-4(Hazardous Substances Data)

1423027-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423027-28-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,0,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1423027-28:
(9*1)+(8*4)+(7*2)+(6*3)+(5*0)+(4*2)+(3*7)+(2*2)+(1*8)=114
114 % 10 = 4
So 1423027-28-4 is a valid CAS Registry Number.

1423027-28-4Relevant articles and documents

Optically pure γ-butyrolactones and epoxy esters via two stereocentered HKR of 3-substituted epoxy esters: A formal synthesis of (-)-paroxetine, Ro 67-8867 and (+)-eldanolide

Devalankar, Dattatray A.,Karabal, Pratibha U.,Sudalai, Arumugam

, p. 1280 - 1285 (2013/05/08)

The HKR of racemic anti- or syn-3-substituted epoxy esters catalyzed by a Co(iii)salen complex provides ready access to the corresponding enantioenriched 3,4-disubstituted γ-butyrolactones and 3-substituted epoxy esters. This strategy has been successfully employed in the formal synthesis of biologically active 3,4-disubstituted piperidine derivatives, (-)-paroxetine and Ro 67-8867 and a natural product, (+)-eldanolide.

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