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CAS

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182439-66-3

N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182439-66-3 Structure

  • Basic information

    1. Product Name: N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide
    2. Synonyms: N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide
    3. CAS NO:182439-66-3
    4. Molecular Formula:
    5. Molecular Weight: 442.514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182439-66-3.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: N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide(182439-66-3)
    11. EPA Substance Registry System: N-[(R)-1-((R)-4-Benzyl-2-oxo-oxazolidine-3-carbonyl)-2,2-diphenyl-ethyl]-acetamide(182439-66-3)

  • 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: 182439-66-3(Hazardous Substances Data)

182439-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182439-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,3 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182439-66:
(8*1)+(7*8)+(6*2)+(5*4)+(4*3)+(3*9)+(2*6)+(1*6)=153
153 % 10 = 3
So 182439-66-3 is a valid CAS Registry Number.

182439-66-3Upstream product

182439-66-3Relevant articles and documents

Cobalt-mediated alkylation of (4R) and (4S)-3-acetoacetyl-4-benzyloxazolidin-2-ones. Preparation of enantiopure diphenylmethyl-, 9-fluorenyl-, and (1-adamantyl)glycines

Galvez, Nicanor,Moreno-Manas, Marcial,Vallribera, Adelina,Molins, Elies,Cabrero, Araceli

, p. 6197 - 6200 (2007/10/03)

The Co(II) complexes of (4R) and (4S)-3-acetoacetyl-4-benzyloxazolidin-2-ones are alkylated diastereoselectively with diphenylmethyl, 9-fluorenyl, and 1-adamantyl bromide. The resulting products are converted into enantiopure α-substituted glycines. Similar results are obtained by alkylation of the free acetoacetyloxazolidinones under Co(II)-catalysis.

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