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CAS

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317322-36-4

2-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 317322-36-4 Structure

  • Basic information

    1. Product Name: 2-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide
    2. Synonyms: 2-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide
    3. CAS NO:317322-36-4
    4. Molecular Formula:
    5. Molecular Weight: 338.406
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 317322-36-4.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-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide(317322-36-4)
    11. EPA Substance Registry System: 2-((4S,5S)-4-benzyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-N-methoxy-N-methyl-acetamide(317322-36-4)

  • 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: 317322-36-4(Hazardous Substances Data)

317322-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 317322-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,2 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 317322-36:
(8*3)+(7*1)+(6*7)+(5*3)+(4*2)+(3*2)+(2*3)+(1*6)=114
114 % 10 = 4
So 317322-36-4 is a valid CAS Registry Number.

317322-36-4Relevant articles and documents

Facile and efficient total synthesis of (+)-preussin.

Lee,Kim,Oh,Ham

, p. 4041 - 4042 (2000)

[structure] The enantioselective total synthesis of (+)-preussin, a potent antifungal agent, has been achieved. The key steps are a Pd(0)-catalyzed oxazoline-forming reaction from L-phenylalanine, hydrogenolysis, and subsequent diastereoselective reductive cyclization of the intermediate aminoketone to pyrrolidine using Pearlman's catalyst.

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