Obtusastyrene

Base Information

• Chemical Name: Obtusastyrene
• CAS No.: 24126-82-7
• Molecular Formula: C15H14 O
• Molecular Weight: 210.276
• Hs Code.: 2907199090
• NSC Number: 154312
• Nikkaji Number: J1.704.544J,J16.150K
• Mol file: 24126-82-7.mol

Synonyms:4-cinnamylphenol;obtusastyrene;obtusastyrene, (E)-isomer

Chemical Property of Obtusastyrene

Chemical Property:

• Vapor Pressure: 7.99E-06mmHg at 25°C
• Boiling Point: 364.5°Cat760mmHg
• Flash Point: 174.7°C
• PSA: 20.23000
• Density: 1.109g/cm³
• LogP: 3.64810
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 210.104465066
• Heavy Atom Count: 16
• Complexity: 208

Purity/Quality:

99% ^*data from raw suppliers

4-Cinnamylphenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C=CCC2=CC=C(C=C2)O
• Isomeric SMILES: C1=CC=C(C=C1)/C=C/CC2=CC=C(C=C2)O

Technology Process of Obtusastyrene

There total 7 articles about Obtusastyrene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

3-methoxy-1-phenylpropene (16277-67-1) + phenol (108-95-2,27073-41-2) → 4-(3-phenyl-2-propen-1-yl)phenol (24126-82-7)

Guidance literature:

With silver hexafluoroantimonate; In 1,2-dichloro-ethane;

DOI:10.1016/j.tetlet.2020.151895

Reference yield: 69.0%

phenyl 3-phenyl-allyl ether (37464-41-8,16519-25-8) + (p-hydroxyphenyl)boronic acid (71597-85-8) → 4-(3-phenyl-2-propen-1-yl)phenol (24126-82-7)

Guidance literature:

With C₂₂H₄₆N₄; palladium diacetate; calcium hydroxide; In N,N-dimethyl acetamide; water; at 20 - 50 ℃; for 24h; Inert atmosphere;

DOI:10.1002/ejoc.201201276

Reference yield: 22.0%

(2E)-3-phenyl-2-propen-1-ol (4407-36-7) + phenol (108-95-2,27073-41-2) → 4-(3-phenyl-2-propen-1-yl)phenol (24126-82-7)

Guidance literature:

With scandium tris(trifluoromethanesulfonate); In 1,2-dichloro-ethane; at 20 ℃; for 0.5h; Reagent/catalyst;

upstream raw materials:

allylbenzene

3-Phenylpropenol

phenol

phenyl 3-phenyl-allyl ether