4-(Allyloxy)-3,5-dichlorobenzaldehyde

Base Information

• Chemical Name: 4-(Allyloxy)-3,5-dichlorobenzaldehyde
• CAS No.: 27164-07-4
• Molecular Formula: C₁₀H₈Cl₂O₂
• Molecular Weight: 231.078
• Hs Code.: 2913000090
• DSSTox Substance ID: DTXSID20366731
• Wikidata: Q82152103
• Mol file: 27164-07-4.mol

Synonyms:4-(ALLYLOXY)-3,5-DICHLOROBENZALDEHYDE;27164-07-4;3,5-dichloro-4-prop-2-enoxybenzaldehyde;AKOS B029005;3,5-dichloro-4-(prop-2-en-1-yloxy)benzaldehyde;Cambridge id 6467884;DTXSID20366731;CBA16407;MFCD02604833;STK187999;AKOS000295024;BS-37472;CS-0116621;SR-01000235302;SR-01000235302-1

Chemical Property of 4-(Allyloxy)-3,5-dichlorobenzaldehyde

Chemical Property:

• Vapor Pressure: 0.000144mmHg at 25°C
• Boiling Point: 332.6°C at 760 mmHg
• Flash Point: 141.8°C
• PSA: 26.30000
• Density: 1.304g/cm³
• LogP: 3.37070
• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 229.9901349
• Heavy Atom Count: 14
• Complexity: 196

Purity/Quality:

99% ^*data from raw suppliers

4-(Allyloxy)-3,5-dichlorobenzaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCOC1=C(C=C(C=C1Cl)C=O)Cl

Technology Process of 4-(Allyloxy)-3,5-dichlorobenzaldehyde

There total 1 articles about 4-(Allyloxy)-3,5-dichlorobenzaldehyde 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:

3,5-dichloro-4-hydroxybenzaldehyde (2314-36-5) + 3-chloroprop-1-ene (107-05-1) → Allyloxy-4-dichloro-3,5-benzaldehyd (27164-07-4)

Guidance literature:

With sodium carbonate; potassium iodide; In ethanol; Heating;

Reference yield:

Allyloxy-4-dichloro-3,5-benzaldehyd (27164-07-4) → 2-(4-Allyloxy-3,5-dichloro-phenyl)-ethylamine (46398-36-1)

Guidance literature:

Multi-step reaction with 2 steps

2: LiAlH₄ / tetrahydrofuran / Heating

With lithium aluminium tetrahydride; In tetrahydrofuran;

upstream raw materials:

3,5-dichloro-4-hydroxybenzaldehyde

3-chloroprop-1-ene

Downstream raw materials:

2-(4-Allyloxy-3,5-dichloro-phenyl)-ethylamine