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565176-85-4

2-Oxazolidinone, 5-[[bis(phenylmethyl)amino]methyl]-3-[3-fluoro-4-(4-morpholinyl)phenyl]-, (5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 565176-85-4 Structure

  • Basic information

    1. Product Name: 2-Oxazolidinone, 5-[[bis(phenylmethyl)amino]methyl]-3-[3-fluoro-4-(4-morpholinyl)phenyl]-, (5S)-
    2. Synonyms:
    3. CAS NO:565176-85-4
    4. Molecular Formula: C28H30FN3O3
    5. Molecular Weight: 475.563
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 565176-85-4.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-Oxazolidinone, 5-[[bis(phenylmethyl)amino]methyl]-3-[3-fluoro-4-(4-morpholinyl)phenyl]-, (5S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Oxazolidinone, 5-[[bis(phenylmethyl)amino]methyl]-3-[3-fluoro-4-(4-morpholinyl)phenyl]-, (5S)-(565176-85-4)
    11. EPA Substance Registry System: 2-Oxazolidinone, 5-[[bis(phenylmethyl)amino]methyl]-3-[3-fluoro-4-(4-morpholinyl)phenyl]-, (5S)-(565176-85-4)

  • 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: 565176-85-4(Hazardous Substances Data)

565176-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 565176-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,5,1,7 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 565176-85:
(8*5)+(7*6)+(6*5)+(5*1)+(4*7)+(3*6)+(2*8)+(1*5)=184
184 % 10 = 4
So 565176-85-4 is a valid CAS Registry Number.

565176-85-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholino phenyl)-isooxazol-2-one

1.2 Other means of identification

Product number -
Other names (S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:565176-85-4 SDS

565176-85-4Relevant articles and documents

METHOD FOR PREPARING LINEZOLID INTERMEDIATE

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Paragraph 0030-0033; 0070-0073, (2015/02/18)

Disclosed is a new method for preparing a methyl substitute of a linezolid intermediate, (S)-2-(3-(3-fluoro-4-morpholinophenyl)-2-oxo-5-oxazoline) (I), wherein the intermediate (I) is obtained by the cyclization of 3-fluoro-4-morpholinophenyl isocyanate (II) and epoxy compound (III). This process has a short process route, low cost, easy operation, and high yield, so is suitable for a large-scale industrial production.

METHOD FOR PREPARING LINEZOLID INTERMEDIATE

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Paragraph 0020; 0021; 0034; 0035, (2015/01/18)

Disclosed is a new method for preparing a methyl substitute of a linezolid intermediate, (S)-2-(3-(3-fluoro-4-morpholinophenyl)-2-oxo-5-oxazoline) (I), wherein the intermediate (I) is obtained by the cyclization of 3-fluoro-4-morpholinophenyl isocyanate (II) and epoxy compound (III). This process has a short process route, low cost, easy operation, and high yield, so is suitable for a large-scale industrial production.

METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF

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, (2011/12/03)

A method for preparing the linezolid (compound 1), which comprises the steps of: (1) carrying out the debenzyl reaction of compound 4 in solvent, to obtain the compound 5 or its acetate; (2) carrying out the acetylation reaction in the amino of the compound 5 or its acetate obtained in step (1) in solvent to obtain the compound 1. The intermediates to prepare the compound 1 and the acetate of compound 5. The present preparation method is easy to obtain the chiral materials and the chiral materials are cheap, the process and the post treatment are simple, the intermediate products and the end product are easy to be purified, the total yield is high, their purities are also high, this preparation method is easy to be used in the industry manufacture.

METHOD FOR PREPARING LINEZOLID AND INTERMEDIATES THEREOF

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Page/Page column 8, (2011/11/13)

A method for preparing the linezolid (compound 1), which comprises the steps of: (1) carrying out the debenzyl reaction of compound 4 in solvent, to obtain the compound 5 or its acetate; (2) carrying out the acetylation reaction in the amino of the compound 5 or its acetate obtained in step (1) in solvent to obtain the compound 1. The intermediates to prepare the compound 1 and the acetate of compound 5. The present preparation method is easy to obtain the chiral materials and the chiral materials are cheap, the process and the post treatment are simple, the intermediate products and the end product are easy to be purified, the total yield is high, their purities are also high, this preparation method is easy to be used in the industry manufacture.

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