4-(4-Ethylphenyl)benzaldehyde

Base Information

• Chemical Name: 4-(4-Ethylphenyl)benzaldehyde
• CAS No.: 101002-44-2
• Molecular Formula: C15H14O
• Molecular Weight: 210.276
• DSSTox Substance ID: DTXSID80362673
• Nikkaji Number: J195.940I
• Wikidata: Q82145975
• Mol file: 101002-44-2.mol

Synonyms:4-(4-ethylphenyl)benzaldehyde;101002-44-2;4'-ETHYLBIPHENYL-4-CARBOXALDEHYDE;4'-Ethyl-[1,1'-biphenyl]-4-carbaldehyde;4'-ethylbiphenyl-4-carbaldehyde;[1,1'-Biphenyl]-4-carboxaldehyde,4'-ethyl-;SCHEMBL2121124;4'-Ethyl-4-biphenylcarbaldehyde;DTXSID80362673;AKOS010262596;4/'-ETHYLBIPHENYL-4-CARBOXALDEHYDE;CS-0439716;FT-0642443;4'-ethylbiphenyl-4-carboxaldehyde, AldrichCPR

Chemical Property of 4-(4-Ethylphenyl)benzaldehyde

Chemical Property:

• Boiling Point: 349.1 °C at 760 mmHg
• Flash Point: 182.3 °C
• PSA: 17.07000
• Density: 1.055 g/cm³
• LogP: 3.72850
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 210.104465066
• Heavy Atom Count: 16
• Complexity: 208

Purity/Quality:

97% ^*data from raw suppliers

4''-Ethylbiphenyl-4-carboxaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1=CC=C(C=C1)C2=CC=C(C=C2)C=O

Technology Process of 4-(4-Ethylphenyl)benzaldehyde

There total 4 articles about 4-(4-Ethylphenyl)benzaldehyde 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: 95.0%

4-ethylphenylboronic acid (63139-21-9) + 4-bromo-benzaldehyde (1122-91-4) → 4′-ethyl-[1,1′-biphenyl]-4-carbaldehyde (101002-44-2)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 130 ℃; for 2h; Catalytic behavior; Green chemistry;

DOI:10.1002/aoc.6415

Reference yield: 86.0%

4-ethylphenylboronic acid (63139-21-9) + 4-chlorobenzaldehyde (104-88-1) → 4′-ethyl-[1,1′-biphenyl]-4-carbaldehyde (101002-44-2)

Guidance literature:

With C₂₃H₂₀ClFeN₃Pd; potassium carbonate; In water; N,N-dimethyl-formamide; at 80 ℃; for 4h; Reagent/catalyst;

DOI:10.1039/c9dt03465j

Reference yield: 85.0%

4-ethylphenylboronic acid (63139-21-9) + 4-bromo-benzaldehyde (1122-91-4) → 4′-ethyl-[1,1′-biphenyl]-4-carbaldehyde (101002-44-2)

Guidance literature:

With C₃₃H₂₆Cl₄OP₂Pd; caesium carbonate; In N,N-dimethyl-formamide; at 110 ℃; for 2h; Reagent/catalyst; Temperature; Time; Solvent;

DOI:10.1016/j.molcata.2014.01.002

upstream raw materials:

4-ethylphenylboronic acid

4-bromo-benzaldehyde

4-chlorobenzaldehyde

Downstream raw materials:

1-((4′-ethyl-[1,1′-biphenyl]-4-yl)methyl)azetidine-3-carboxylic acid

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