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4-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 287719-11-3 Structure
  • Basic information

    1. Product Name: 4-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester
    2. Synonyms: 4-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester
    3. CAS NO:287719-11-3
    4. Molecular Formula:
    5. Molecular Weight: 409.482
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 287719-11-3.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-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester(287719-11-3)
    11. EPA Substance Registry System: 4-(4-benzhydryl-2-oxo-oxazolidin-3-yl)-4-oxo-butyric acid tert-butyl ester(287719-11-3)
  • 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: 287719-11-3(Hazardous Substances Data)

287719-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287719-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,7,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 287719-11:
(8*2)+(7*8)+(6*7)+(5*7)+(4*1)+(3*9)+(2*1)+(1*1)=183
183 % 10 = 3
So 287719-11-3 is a valid CAS Registry Number.

287719-11-3Relevant articles and documents

A new methodology for the synthesis of β-amino acids

Sibi, Mukund P.,Deshpande, Prasad K.

, p. 1461 - 1466 (2000)

A differentially functionalized succinic acid unit 6 undergoes alkylation with excellent regio- and high stereocontrol at the carbon α to the imide to furnish the alkylated product 7 in 60-83% yield. Selective removal of the imide provides 8 in 80-90% yie

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