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CAS

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1583260-39-2

(3S,4R)-isopropyl 5-(benzyloxy)-2,2-difluoro-3-hydroxy-4-(2,2,6,6-tetramethylpiperidin-1-yloxy)pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1583260-39-2 Structure

  • Basic information

    1. Product Name: (3S,4R)-isopropyl 5-(benzyloxy)-2,2-difluoro-3-hydroxy-4-(2,2,6,6-tetramethylpiperidin-1-yloxy)pentanoate
    2. Synonyms:
    3. CAS NO:1583260-39-2
    4. Molecular Formula:
    5. Molecular Weight: 457.558
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1583260-39-2.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: (3S,4R)-isopropyl 5-(benzyloxy)-2,2-difluoro-3-hydroxy-4-(2,2,6,6-tetramethylpiperidin-1-yloxy)pentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,4R)-isopropyl 5-(benzyloxy)-2,2-difluoro-3-hydroxy-4-(2,2,6,6-tetramethylpiperidin-1-yloxy)pentanoate(1583260-39-2)
    11. EPA Substance Registry System: (3S,4R)-isopropyl 5-(benzyloxy)-2,2-difluoro-3-hydroxy-4-(2,2,6,6-tetramethylpiperidin-1-yloxy)pentanoate(1583260-39-2)

  • 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: 1583260-39-2(Hazardous Substances Data)

1583260-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1583260-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,3,2,6 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1583260-39:
(9*1)+(8*5)+(7*8)+(6*3)+(5*2)+(4*6)+(3*0)+(2*3)+(1*9)=172
172 % 10 = 2
So 1583260-39-2 is a valid CAS Registry Number.

1583260-39-2Downstream Products

1583260-39-2Relevant articles and documents

A general and enantioselective approach to pentoses: A rapid synthesis of PSI-6130, the nucleoside core of sofosbuvir

Peifer, Manuel,Berger, Rapha?lle,Shurtleff, Valerie W.,Conrad, Jay C.,Macmillan, David W. C.

supporting information, p. 5900 - 5903 (2014/05/20)

An efficient route towards biologically relevant pentose derivatives is described. The de novo synthetic strategy features an enantioselective α-oxidation reaction enabled by a chiral amine in conjunction with copper(II) catalysis. A subsequent Mukaiyama aldol coupling allows for the incorporation of a wide array of modular two-carbon fragments. Lactone intermediates accessed via this route provide a useful platform for elaboration, as demonstrated by the preparation of a variety of C-nucleosides and fluorinated pentoses. Finally, this work has facilitated expedient syntheses of pharmaceutically active compounds currently in clinical use.

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