4-(4-Chloro-3-methylphenoxy)phenol

Base Information

• Chemical Name: 4-(4-Chloro-3-methylphenoxy)phenol
• CAS No.: 40843-52-5
• Molecular Formula: C₁₃H₁₁ClO₂
• Molecular Weight: 234.682
• Hs Code.: 2909500000
• DSSTox Substance ID: DTXSID50509376
• Wikidata: Q82366885
• Mol file: 40843-52-5.mol

Synonyms:4-(4-CHLORO-3-METHYLPHENOXY)PHENOL;40843-52-5;Phenol,4-(4-chloro-3-methylphenoxy)-;SCHEMBL11179365;DTXSID50509376

Chemical Property of 4-(4-Chloro-3-methylphenoxy)phenol

Chemical Property:

• Vapor Pressure: 1.45E-05mmHg at 25°C
• Boiling Point: 356.1°C at 760 mmHg
• PKA: 9.92±0.15(Predicted)
• Flash Point: 169.2°C
• PSA: 29.46000
• Density: 1.257g/cm³
• LogP: 4.14630
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 234.0447573
• Heavy Atom Count: 16
• Complexity: 214

Purity/Quality:

99%min ^*data from raw suppliers

4-(4-Chloro-3-methylphenoxy)phenol AldrichCPR ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=CC(=C1)OC2=CC=C(C=C2)O)Cl

Technology Process of 4-(4-Chloro-3-methylphenoxy)phenol

There total 5 articles about 4-(4-Chloro-3-methylphenoxy)phenol 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:

4-Chloro-3-methylphenol (59-50-7) → 4-(4-Chlor-3-methylphenoxy)-phenol (40843-52-5)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃ / N,N-dimethyl-acetamide / Heating

2: mCPBA

With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In N,N-dimethyl acetamide; 2: Baeyer-Villiger oxidation;

DOI:10.1016/S0960-894X(03)00505-5

Reference yield:

4-fluorobenzaldehyde (459-57-4) → 4-(4-Chlor-3-methylphenoxy)-phenol (40843-52-5)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃ / N,N-dimethyl-acetamide / Heating

2: mCPBA

With potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In N,N-dimethyl acetamide; 2: Baeyer-Villiger oxidation;

DOI:10.1016/S0960-894X(03)00505-5

Reference yield:

4-(4-Chlor-3-methylphenoxy)-anisol (40843-51-4) → 4-(4-Chlor-3-methylphenoxy)-phenol (40843-52-5)

Guidance literature:

With hydrogen bromide; In acetic acid;

upstream raw materials:

4-(4-Chlor-3-methylphenoxy)-anisol

4-(4-Chloro-3-methyl-phenoxy)-benzaldehyde

4-Chloro-3-methylphenol

4-fluorobenzaldehyde

Downstream raw materials:

4-Amino-2-[4-(4-chloro-3-methyl-phenoxy)-phenoxy]-butyric acid

2-[4-(4-Chloro-3-methyl-phenoxy)-phenoxy]-propionic acid

4-(4-Allyloxy-phenoxy)-1-chloro-2-methyl-benzene

(3-{3-[4-(4-chloro-3-methyl-phenoxy)-2-propyl-phenoxy]-propoxy}-phenyl)-hydroxy-acetic acid methyl ester

Refernces