2-Iodo-1-phenyl-phenanthrene

Base Information

• Chemical Name: 2-Iodo-1-phenyl-phenanthrene
• CAS No.: 41790-93-6
• Molecular Formula: C20H13I
• Molecular Weight: 380.22169
• Hs Code.: 2903999090
• DSSTox Substance ID: DTXSID30467920
• Wikidata: Q82295008
• Mol file: 41790-93-6.mol

Synonyms:2-iodo-1-phenyl-phenanthrene;41790-93-6;DTXSID30467920;KUC100643N;AKOS015965714

Chemical Property of 2-Iodo-1-phenyl-phenanthrene

Chemical Property:

• PSA: 0.00000
• LogP: 6.26460
• XLogP3: 6.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 380.00620
• Heavy Atom Count: 21
• Complexity: 346

Purity/Quality:

2-IODO-1-PHENYL-PHENANTHRENE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=C(C=CC3=C2C=CC4=CC=CC=C43)I

Technology Process of 2-Iodo-1-phenyl-phenanthrene

There total 3 articles about 2-Iodo-1-phenyl-phenanthrene 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%

1-(1-naphthyl)-4-phenylbut-3-yn-2-ol (874338-50-8) → 2-iodo-1-phenylphenanthrene (41790-93-6)

Guidance literature:

With iodine; sodium hydrogencarbonate; In acetonitrile; at 20 ℃;

DOI:10.1021/jo051948k

Reference yield:

1-((Z)-4-Phenyl-but-1-en-3-ynyl)-naphthalene → 2-iodo-1-phenylphenanthrene (41790-93-6)

Guidance literature:

With iodine; In benzene; Irradiation;

DOI:10.1039/P29760001115

Reference yield:

→ 2-iodo-1-phenylphenanthrene (41790-93-6)

Guidance literature:

1-(α-Naphthyl)-4-phenylbut-1-en-3-in (I), hν in Benzol m. I2;

DOI:10.1016/S0040-4039(01)95723-5

upstream raw materials:

1-(1-naphthyl)-4-phenylbut-3-yn-2-ol

Downstream raw materials:

1,2-diphenylphenanthrene

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