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4-Isopropylcatechol

Base Information Edit
  • Chemical Name:4-Isopropylcatechol
  • CAS No.:2138-43-4
  • Molecular Formula:C9H12 O2
  • Molecular Weight:152.193
  • Hs Code.:2907299090
  • European Community (EC) Number:218-384-5
  • NSC Number:62676
  • UNII:SE856V0X6N
  • DSSTox Substance ID:DTXSID20175643
  • Nikkaji Number:J51.424A
  • Wikidata:Q27289157
  • Mol file:2138-43-4.mol
4-Isopropylcatechol

Synonyms:4-isopropylcatechol

Suppliers and Price of 4-Isopropylcatechol
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
  • TRC
  • 4-Isopropylcatechol
  • 50mg
  • $ 210.00
Total 18 raw suppliers
Chemical Property of 4-Isopropylcatechol Edit
Chemical Property:
  • Vapor Pressure:0.00399mmHg at 25°C 
  • Melting Point:78°C 
  • Refractive Index:1.4440 (estimate) 
  • Boiling Point:271°Cat760mmHg 
  • PKA:9.86±0.10(Predicted) 
  • Flash Point:129.2°C 
  • PSA:40.46000 
  • Density:1.116g/cm3 
  • LogP:2.22120 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Acetonitrile (Slightly), Chloroform (Slightly) 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:152.083729621
  • Heavy Atom Count:11
  • Complexity:123
Purity/Quality:

99.9% *data from raw suppliers

4-Isopropylcatechol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1=CC(=C(C=C1)O)O
  • Uses 4-Isopropylcatechol was used in a catalytic aerobic cross-?dehydrogenative coupling (CDC) reaction with phenols to make aryl ethers.
Technology Process of 4-Isopropylcatechol

There total 15 articles about 4-Isopropylcatechol 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 dihydrogen peroxide; In sodium hydroxide; for 0.5h; <45 deg C;
Guidance literature:
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In N,N-dimethyl-formamide; at 20 - 23 ℃; for 4h;
DOI:10.1002/anie.201606359
Guidance literature:
With iron(III) trifluoromethanesulfonate; dihydrogen peroxide; C26H42N4O10S2; chloroacetic acid; In water; acetonitrile; at 25 ℃; for 1h;
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