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4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 352524-61-9 Structure
  • Basic information

    1. Product Name: 4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde
    2. Synonyms: 4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde
    3. CAS NO:352524-61-9
    4. Molecular Formula:
    5. Molecular Weight: 368.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 352524-61-9.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: 4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde(352524-61-9)
    11. EPA Substance Registry System: 4-((5S)-5-((1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)methyl)-2-oxo-1,3-oxazolidin-3-yl)-2-fluorobenzaldehyde(352524-61-9)
  • 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: 352524-61-9(Hazardous Substances Data)

352524-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 352524-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,2 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 352524-61:
(8*3)+(7*5)+(6*2)+(5*5)+(4*2)+(3*4)+(2*6)+(1*1)=129
129 % 10 = 9
So 352524-61-9 is a valid CAS Registry Number.

352524-61-9Relevant articles and documents

The synthesis and biological evaluation of a novel series of antimicrobials of the oxazolidinone class.

Sciotti, Richard J,Pliushchev, Marina,Wiedeman, Paul E,Balli, Darlene,Flamm, Robert,Nilius, Angela M,Marsh, Kennan,Stolarik, DeAnne,Jolly, Robert,Ulrich, Roger,Djuric, Stevan W

, p. 2121 - 2123 (2002)

A novel series of antimicrobials of the oxazolidinone class is disclosed. These compounds are characterized relative to previously described analogues by a 'halostilbene-derived' pharmacophore and demonstrate enhanced antimicrobial activity against key Gram-positive pathogens when compared to Linezolid.

OXAZOLIDINONE CHEMOTHERAPEUTIC AGENTS

-

, (2008/06/13)

Compounds of the formula or therapeutically acceptable salts or prodrugs thereof, are useful for treating bacterial infections, psoriasis, arthritis, and toxicity due to chemotherapy. Preparation of the compounds, compositions containing the compounds, an

Oxazolidinone chemotherapeutic agents

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts or prodrugs thereof, are useful for treating bacterial infections, psoriasis, arthritis, and toxicity due to chemotherapy. Preparation of the compounds, compositions containing the compounds, an

Synthesis of N-arylated oxazolidinones via a palladium catalyzed cross coupling reaction. Application to the synthesis of the antibacterial agent Dup-721

Madar, David J.,Kopecka, Hana,Pireh, Daisy,Pease, Jonathan,Pliushchev, Marina,Sciotti, Richard J.,Wiedeman, Paul E.,Djuric, Stevan W.

, p. 3681 - 3684 (2007/10/03)

A method for the intermolecular coupling of aryl bromides and oxazolidinones is described. Application to intermediates useful for the preparation of a known class of antibacterial agent and the synthesis of the known antibacterial oxazolidinone Dup-721 are described.

Oxazolidinone chemotherapeutic agents

-

, (2008/06/13)

Compounds of formula (I) or therapeutically acceptable salts or prodrugs thereof, are useful for treating bacterial infections, psoriasis, arthritis, and toxicity due to chemotherapy. Preparation of the compounds, compositions containing the compounds, an

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