3-(2-Hydroxy-3,5-dichlorophenyl)prop-1-ene

Base Information

• Chemical Name: 3-(2-Hydroxy-3,5-dichlorophenyl)prop-1-ene
• CAS No.: 19182-95-7
• Molecular Formula: C9H8Cl2O
• Molecular Weight: 203.068
• DSSTox Substance ID: DTXSID40493674
• Nikkaji Number: J2.465.577F
• Wikidata: Q82340533
• Mol file: 19182-95-7.mol

Synonyms:19182-95-7;2,4-Dichloro-6-(prop-2-en-1-yl)phenol;3-(2-hydroxy-3,5-dichlorophenyl)prop-1-ene;2-Allyl-4,6-dichlorophenol;SCHEMBL10400341;DTXSID40493674;2,4-dichloro-6-prop-2-enylphenol;AKOS005353828;F96953

Chemical Property of 3-(2-Hydroxy-3,5-dichlorophenyl)prop-1-ene

Chemical Property:

• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 201.9952203
• Heavy Atom Count: 12
• Complexity: 161

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

Technology Process of 3-(2-Hydroxy-3,5-dichlorophenyl)prop-1-ene

There total 6 articles about 3-(2-Hydroxy-3,5-dichlorophenyl)prop-1-ene 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: 92.0%

1-(allyloxy)-2,4-dichlorobenzene (5441-16-7) → 3-(2-hydroxy-3,5-dichlorophenyl)prop-1-ene (19182-95-7)

Guidance literature:

at 245 - 250 ℃; for 0.166667h;

DOI:10.1021/jm00371a003

Reference yield:

methyl 3,5-dichlorosalicylate (7606-87-3) → 3-(2-hydroxy-3,5-dichlorophenyl)prop-1-ene (19182-95-7)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate; methylethyl ketone

2: methanolic NaOH-solution

With sodium hydroxide; potassium carbonate; 2,4-dimethylpentan-3-one;

Reference yield:

2-allyloxy-3,5-dichloro-benzoic acid methyl ester → 3-(2-hydroxy-3,5-dichlorophenyl)prop-1-ene (19182-95-7)

Guidance literature:

Multi-step reaction with 2 steps

1: methanolic NaOH-solution

With sodium hydroxide;

upstream raw materials:

1-(allyloxy)-2,4-dichlorobenzene

2-allyloxy-3,5-dichloro-benzoic acid

methyl 3,5-dichlorosalicylate

methyl salicylate

Downstream raw materials:

(E/Z)-2,4-dichloro-6-(prop-1-enyl)phenol

1-(2-hydroxy-3,5-dichlorophenyl)-2,3-epoxypropane

2-acetoxy-1,5-dichloro-3-(2,3-dibromo-propyl)-benzene