Welcome to LookChem.com Sign In|Join Free

CAS

  • or

854545-92-9

(3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

854545-92-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 854545-92-9 Structure

  • Basic information

    1. Product Name: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol
    2. Synonyms: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol
    3. CAS NO:854545-92-9
    4. Molecular Formula:
    5. Molecular Weight: 241.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 854545-92-9.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: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol(854545-92-9)
    11. EPA Substance Registry System: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-6-yl)methanol(854545-92-9)

  • 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: 854545-92-9(Hazardous Substances Data)

854545-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854545-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,5,4 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 854545-92:
(8*8)+(7*5)+(6*4)+(5*5)+(4*4)+(3*5)+(2*9)+(1*2)=199
199 % 10 = 9
So 854545-92-9 is a valid CAS Registry Number.

854545-92-9Relevant articles and documents

Complementary multiple hydrogen bonding interactions induce the self-assembly of supramolecular structures from heteronucleobase-functionalized benzoxazine and polyhedral oligomeric silsesquioxane nanoparticles

Hu, Wei-Hsun,Huang, Kai-Wei,Chiou, Chin-Wei,Kuo, Shiao-Wei

, p. 9020 - 9028 (2012)

We prepared octuply adenine (A)-functionalized polyhedral oligomeric silsesquioxane [(octakis(vinylbenzyladenine-siloxy)silsesquioxane, OBA-POSS] nanoparticles through the reaction of A with octakis(benzyl chloride) POSS (OVBC-POSS), itself prepared through hydrosilylation of octakis(dimethylsiloxy) silsesquioxane (Q8M8H) with vinyl benzyl chloride. We observed the self-assembly of lamellar structures from the complexation of a thymine (T)-functionalized polybenzoxazine (PA-T) with OBA-POSS, stabilized through complementary multiple hydrogen bonding interactions between the T groups of PA-T and the A groups of OBA-POSS. In addition, incorporating POSS presenting multiple, strong, complementary hydrogen bonding A units into the PA-T matrix significantly enhanced the thermal stability of this polymer, as evidenced using differential scanning calorimetry and thermogravimetric analysis.

A Cross-Linkable Electron-Transport Layer Based on a Fullerene?Benzoxazine Derivative for Inverted Polymer Solar Cells

Deb, Biswapriya,Joseph, Joshy,Ravi, Remya,Vittala, Sandeepa Kulala

, p. 1534 - 1541 (2020)

The synthesis, optoelectronic characterization and device properties of a cross-linkable fullerene derivative, [6,6]-phenyl-C61-butyric benzoxazine ester (PCBB) is reported. PCBB shows all the basic photophysical and electrochemical properties

Examining the effect of hydroxyl groups on the thermal properties of polybenzoxazines: Using molecular design and Monte Carlo simulation

Zhang, Kan,Han, Lu,Nie, Yijing,Szigeti, Matthew Louis,Ishida, Hatsuo

, p. 18038 - 18050 (2018)

The influence of methylol and phenolic hydroxyl on the thermal properties of polybenzoxazines has been studied using two monofunctional benzoxazine monomers synthesized from para methylol-/ethyl- phenol, aniline and paraformaldehyde. The chemical structur

BENZOXAZINE BLENDS

-

Paragraph 0181, (2021/05/21)

Provided herein are blends of benzoxazine-containing monomers with polymer having one or more leaving groups, such as tosylated polymers (e.g., tosylated polyethylene glycol (PEG)); or blends of benzoxazine-containing monomers with particles/fibers having

Mechanistic pathways for the polymerization of methylol-functional benzoxazine monomers

Baqar, Mohamed,Agag, Tarek,Huang, Rongzhi,Maia, Joao,Qutubuddin, Syed,Ishida, Hatsuo

, p. 8119 - 8125 (2013/01/15)

The polymerization mechanism of methylol-functional benzoxazine monomers is reported using a series of monofunctional benzoxazine monomers synthesized via a condensation reaction of ortho-, meta-, or para-methylol-phenol, aniline, and paraformaldehyde fol

Methacryloyl-functional benzoxazine: Photopolymerization and thermally activated polymerization

Jin, Lin,Agag, Tarek,Yagci, Yusuf,Ishida, Hatsuo

experimental part, p. 767 - 772 (2012/02/01)

A novel class of photopolymerizable benzoxazines has been developed. This class has been coined as methacryloyl-functional benzoxazines. It has been synthesized by the reaction of the new benzoxazine monomers: (3-phenyl-3,4-dihydro-2H-benzo[e][1,3]oxazin-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 854545-92-9