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CAS

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19029-49-3

2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 19029-49-3 Structure

  • Basic information

    1. Product Name: 2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine
    2. Synonyms: 2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine
    3. CAS NO:19029-49-3
    4. Molecular Formula:
    5. Molecular Weight: 237.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19029-49-3.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: 2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine(19029-49-3)
    11. EPA Substance Registry System: 2,6-diphenyl-3,6-dihydro-2H-[1,2]oxazine(19029-49-3)

  • 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: 19029-49-3(Hazardous Substances Data)

19029-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19029-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19029-49:
(7*1)+(6*9)+(5*0)+(4*2)+(3*9)+(2*4)+(1*9)=113
113 % 10 = 3
So 19029-49-3 is a valid CAS Registry Number.

19029-49-3Downstream Products

19029-49-3Relevant articles and documents

Lewis acid catalyzed reactivity switch: Pseudo three-component annulation of nitrosoarenes and (epoxy)styrenes

Purkait, Anisha,Saha, Subhajit,Ghosh, Santanu,Jana, Chandan K.

, p. 15032 - 15035 (2020)

A Lewis acid catalyzed annulation reaction via arene functionalization of nitrosoarenes and C-C cleavage of (epoxy)styrene to provide arylquinolines is reported. The Lewis acid catalyst altered the annulation pattern providing arylquinolines instead of oxazolidines. The reaction with styrene resulted in a mixture of 2,4-diarylquinoline and 4-Arylquinoline, while only 3-Arylquinoline was formed from the reaction of epoxystyrene. This journal is

Copper-catalyzed pyrrole synthesis from 3,6-dihydro-1,2-oxazines

Yasukawa, Naoki,Kuwata, Marina,Imai, Takuya,Monguchi, Yasunari,Sajiki, Hironao,Sawama, Yoshinari

supporting information, p. 4409 - 4413 (2018/10/17)

Highly-functionalized pyrroles could be effectively synthesized from 3,6-dihydro-1,2-oxazines using a heterogeneous copper on carbon (Cu/C) under neat heating conditions. Furthermore, the in situ formation of 3,6-dihydro-1,2-oxazines via the hetero Diels-Alder reaction between nitroso dienophiles and 1,3-dienes and the following Cu/C-catalyzed pyrrole synthesis also provided the corresponding pyrrole derivatives in a one-pot manner.

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