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1567264-93-0

5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1567264-93-0 Structure

  • Basic information

    1. Product Name: 5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one
    2. Synonyms: 5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one
    3. CAS NO:1567264-93-0
    4. Molecular Formula:
    5. Molecular Weight: 278.308
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1567264-93-0.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: 5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one(1567264-93-0)
    11. EPA Substance Registry System: 5-(2-nitrobenzyl)-3-tertbutyloxazolidin-2-one(1567264-93-0)

  • 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: 1567264-93-0(Hazardous Substances Data)

1567264-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1567264-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,7,2,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1567264-93:
(9*1)+(8*5)+(7*6)+(6*7)+(5*2)+(4*6)+(3*4)+(2*9)+(1*3)=200
200 % 10 = 0
So 1567264-93-0 is a valid CAS Registry Number.

1567264-93-0Downstream Products

1567264-93-0Relevant articles and documents

A novel one-pot synthesis of oxazolidinones through direct introduction of CO2 into allylamine derivatives

Soldi, Laura,Massera, Chiara,Costa, Mirco,Della Ca', Nicola

, p. 1379 - 1383 (2014)

1,3-Oxazolindin-2-one derivatives were obtained for the first time through carboxylative cyclization of allylamines in the absence of any metal or base catalyst. An electron-withdrawing substituent on the allylic double bond is crucial for the reaction success. Allylamines react with CO2 in MeCN/MeOH mixture and in scCO2 giving satisfactory results.

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