2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole

Base Information

• Chemical Name: 2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole
• CAS No.: 1248-45-9
• Molecular Formula: C24H16 N2 O
• Molecular Weight: 348.404
• Hs Code.: 2934999090
• European Community (EC) Number: 215-001-3
• DSSTox Substance ID: DTXSID10154487
• Nikkaji Number: J217.079E
• Wikidata: Q83021743
• Mol file: 1248-45-9.mol

Synonyms:1248-45-9;EINECS 215-001-3;2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole;2-naphthalen-1-yl-5-(4-phenylphenyl)-1,3,4-oxadiazole;2-(4-Biphenylyl)-5-(1-naphthyl)-1,3,4-oxadiazole;2-[1,1'-Biphenyl]-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole;2-[1,1/'-biphenyl]-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole;1,3,4-Oxadiazole, 2-[1,1'-biphenyl]-4-yl-5-(1-naphthalenyl)-;1,3,4-Oxadiazole, 2-(1,1'-biphenyl)-4-yl-5-(1-naphthalenyl)-;SCHEMBL19932454;DTXSID10154487;2-(1-Naphthyl)-5-(4-biphenylyl)-l,3,4-oxadiazol

Chemical Property of 2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole

Chemical Property:

• Boiling Point: 561.4°Cat760mmHg
• Flash Point: 290.9°C
• PSA: 38.92000
• Density: 1.207g/cm³
• LogP: 6.22380
• XLogP3: 6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 348.126263138
• Heavy Atom Count: 27
• Complexity: 469

Purity/Quality:

99% ^*data from raw suppliers

2-(1-Naphthyl-5-(4-biphenylyl))-1,3,4-oxadiazole ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)C3=NN=C(O3)C4=CC=CC5=CC=CC=C54

Technology Process of 2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole

There total 4 articles about 2-(1,1'-Biphenyl)-4-yl-5-(1-naphthyl)-1,3,4-oxadiazole 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:

N-(biphenyl-4-carbonyl)-N'-[1]naphthoyl-hydrazine (6781-70-0) → 2-biphenyl-4-yl-5-naphthalen-1-yl-[1,3,4]oxadiazole (1248-45-9)

Guidance literature:

With trichlorophosphate;

Reference yield:

4-phenylbenzohydrazide (18622-23-6) → 2-biphenyl-4-yl-5-naphthalen-1-yl-[1,3,4]oxadiazole (1248-45-9)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine

2: POCl₃

With pyridine; trichlorophosphate;

Reference yield:

naphthalene-1-carbonic acid chloride (879-18-5) → 2-biphenyl-4-yl-5-naphthalen-1-yl-[1,3,4]oxadiazole (1248-45-9)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine

2: POCl₃

With pyridine; trichlorophosphate;

upstream raw materials:

N-(biphenyl-4-carbonyl)-N'-[1]naphthoyl-hydrazine

4-phenylbenzohydrazide

naphthalene-1-carbonic acid chloride