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1-Chloro-3-(pentyloxy)benzene

Base Information Edit
  • Chemical Name:1-Chloro-3-(pentyloxy)benzene
  • CAS No.:51241-38-4
  • Molecular Formula:C11H15ClO
  • Molecular Weight:198.68900
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50707613
  • Nikkaji Number:J156.463C
  • Wikidata:Q82641484
  • Mol file:51241-38-4.mol
1-Chloro-3-(pentyloxy)benzene

Synonyms:1-CHLORO-3-(PENTYLOXY)BENZENE;51241-38-4;3-Chlorophenylpentyl ether;SCHEMBL8551026;3-Chlorophenol, n-pentyl ether;DTXSID50707613;KESDBEGYAQDHHZ-UHFFFAOYSA-N;AKOS014092287

Suppliers and Price of 1-Chloro-3-(pentyloxy)benzene
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 0 raw suppliers
Chemical Property of 1-Chloro-3-(pentyloxy)benzene Edit
Chemical Property:
  • Boiling Point:261.9±13.0 °C(Predicted) 
  • PSA:9.23000 
  • Density:1.038±0.06 g/cm3(Predicted) 
  • LogP:3.90900 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:5
  • Exact Mass:198.0811428
  • Heavy Atom Count:13
  • Complexity:127
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCOC1=CC(=CC=C1)Cl
Technology Process of 1-Chloro-3-(pentyloxy)benzene

There total 1 articles about 1-Chloro-3-(pentyloxy)benzene 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:
Guidance literature:
With potassium hydroxide; PEG-6000; at 150 ℃; for 6h;
DOI:10.1016/S0040-4020(01)91597-2
Guidance literature:
Multi-step reaction with 2 steps
1: aluminum (III) chloride / dichloromethane / 2 h / 5 - 20 °C / Inert atmosphere
2: hydroxylamine hydrochloride / ethanol / 5 h / Reflux; Inert atmosphere
With aluminum (III) chloride; hydroxylamine hydrochloride; In ethanol; dichloromethane; 1: |Friedel-Crafts Acylation;
DOI:10.1039/c3nj00032j
Guidance literature:
Multi-step reaction with 6 steps
1: aluminum (III) chloride / dichloromethane / 2 h / 5 - 20 °C / Inert atmosphere
2: hydroxylamine hydrochloride / ethanol / 5 h / Reflux; Inert atmosphere
3: sodium tetrahydroborate; iodine / tetrahydrofuran / 7.5 h / 0 °C / Reflux; Inert atmosphere
4: triethylamine / tetrahydrofuran / 2 h / 5 - 20 °C / Inert atmosphere
5: thionyl chloride / toluene / 3 h / 80 °C / Inert atmosphere
6: sodium hydroxide / methanol / 1 h / 50 °C / Inert atmosphere
With aluminum (III) chloride; sodium tetrahydroborate; thionyl chloride; hydroxylamine hydrochloride; iodine; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; toluene; 1: |Friedel-Crafts Acylation;
DOI:10.1039/c3nj00032j
upstream raw materials:

pentan-1-ol

1,3-Dichlorobenzene

Downstream raw materials:

C15H20ClNO4

C20H20ClF2NO2

C20H21Cl2F2NO2

C20H22ClF2NO3

Refernces Edit
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