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185342-17-0

2-Oxazolidinone, 3-[(3-chloro-4-methoxyphenyl)acetyl]-4-methyl-5-phenyl-, (4R,5S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 185342-17-0 Structure

  • Basic information

    1. Product Name: 2-Oxazolidinone, 3-[(3-chloro-4-methoxyphenyl)acetyl]-4-methyl-5-phenyl-, (4R,5S)-
    2. Synonyms:
    3. CAS NO:185342-17-0
    4. Molecular Formula: C19H18ClNO4
    5. Molecular Weight: 359.809
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 185342-17-0.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, 3-[(3-chloro-4-methoxyphenyl)acetyl]-4-methyl-5-phenyl-, (4R,5S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Oxazolidinone, 3-[(3-chloro-4-methoxyphenyl)acetyl]-4-methyl-5-phenyl-, (4R,5S)-(185342-17-0)
    11. EPA Substance Registry System: 2-Oxazolidinone, 3-[(3-chloro-4-methoxyphenyl)acetyl]-4-methyl-5-phenyl-, (4R,5S)-(185342-17-0)

  • 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: 185342-17-0(Hazardous Substances Data)

185342-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 185342-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,3,4 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 185342-17:
(8*1)+(7*8)+(6*5)+(5*3)+(4*4)+(3*2)+(2*1)+(1*7)=140
140 % 10 = 0
So 185342-17-0 is a valid CAS Registry Number.

185342-17-0Relevant articles and documents

Ruthenium-promoted diaryl ether synthesis in the construction of the F- O-G ring system of a teicoplanin model

Pearson, Anthony J.,Belmont, Philippe O.

, p. 1671 - 1675 (2007/10/03)

An end-game approach is described for the synthesis of glycopeptide antibiotics related to teicoplanin, using ruthenium-promoted diaryl ether formation, followed by cycloamidation. (C) 2000 Elsevier Science Ltd.

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