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CAS

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1423027-17-1

((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1423027-17-1 Structure

  • Basic information

    1. Product Name: ((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate
    2. Synonyms: ((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate
    3. CAS NO:1423027-17-1
    4. Molecular Formula:
    5. Molecular Weight: 288.297
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1423027-17-1.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: ((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate(1423027-17-1)
    11. EPA Substance Registry System: ((2R,3S)-3-(4-fluorophenyl)-5-oxotetrahydrofuran-2-yl)methyl methanesulfonate(1423027-17-1)

  • 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: 1423027-17-1(Hazardous Substances Data)

1423027-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423027-17-1 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, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1423027-17:
(9*1)+(8*4)+(7*2)+(6*3)+(5*0)+(4*2)+(3*7)+(2*1)+(1*7)=111
111 % 10 = 1
So 1423027-17-1 is a valid CAS Registry Number.

1423027-17-1Relevant 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

supporting information, 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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