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28819-48-9

2H-1,3-Oxazine, tetrahydro-2,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28819-48-9 Structure

  • Basic information

    1. Product Name: 2H-1,3-Oxazine, tetrahydro-2,3-diphenyl-
    2. Synonyms:
    3. CAS NO:28819-48-9
    4. Molecular Formula: C16H17NO
    5. Molecular Weight: 239.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28819-48-9.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: 2H-1,3-Oxazine, tetrahydro-2,3-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2H-1,3-Oxazine, tetrahydro-2,3-diphenyl-(28819-48-9)
    11. EPA Substance Registry System: 2H-1,3-Oxazine, tetrahydro-2,3-diphenyl-(28819-48-9)

  • 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: 28819-48-9(Hazardous Substances Data)

28819-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28819-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28819-48:
(7*2)+(6*8)+(5*8)+(4*1)+(3*9)+(2*4)+(1*8)=149
149 % 10 = 9
So 28819-48-9 is a valid CAS Registry Number.

28819-48-9Downstream Products

28819-48-9Relevant articles and documents

The synthesis of new 1,3-oxazolidines and 1,3-oxazinanes containing (η6-arene)tricarbonylchromium group based on condensation between aldehydes and amino alcohols

Artemov,Sazonova,Krylova,Zvereva,Pechen,Fukin,Cherkasov,Faerman,Grishina, N. Yu.

, p. 884 - 892 (2018)

The condensation reactions of β- and γ-amino alcohols containing phenyl or (η6-arene) tricarbonylchromium substituent with formaldehyde, acetaldehyde, benzaldehyde, and (η6-benzaldehyde)tricarbonylchromium were studied. The resulting 1,3-oxazolidine and 1,3-oxazinane products were isolated in a pure form and identified by different physicochemical methods. The effect of (η6-arene)tricarbonylchromium moiety on the reaction process was demonstrated.

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