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2,4,6-Triisopropylbenzenesulfonyl chloride

Base Information Edit
  • Chemical Name:2,4,6-Triisopropylbenzenesulfonyl chloride
  • CAS No.:6553-96-4
  • Molecular Formula:C15H23ClO2S
  • Molecular Weight:302.865
  • Hs Code.:29049020
  • European Community (EC) Number:229-479-6
  • NSC Number:102803
  • UNII:4QZ3QZX6G4
  • DSSTox Substance ID:DTXSID30215827
  • Nikkaji Number:J124.143E
  • Wikidata:Q72513624
  • Mol file:6553-96-4.mol
2,4,6-Triisopropylbenzenesulfonyl chloride

Synonyms:2,4,6-TIPBS;2,4,6-triisopropylbenzenesulfonyl;2,4,6-triisopropylbenzenesulfonyl chloride

Suppliers and Price of 2,4,6-Triisopropylbenzenesulfonyl chloride
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
  • Usbiological
  • 2,4,6-Triisopropylbenzenesulfonyl chloride
  • 50g
  • $ 355.00
  • TRC
  • 2,4,6-Triisopropylbenzenesulfonyl chloride
  • 100g
  • $ 250.00
  • TCI Chemical
  • 2,4,6-Triisopropylbenzenesulfonyl Chloride >97.0%(T)
  • 500g
  • $ 264.00
  • TCI Chemical
  • 2,4,6-Triisopropylbenzenesulfonyl Chloride >97.0%(T)
  • 25g
  • $ 21.00
  • SynQuest Laboratories
  • 2,4,6-Tris(isopropyl)benzenesulfonyl chloride 98.0%
  • 25 g
  • $ 23.00
  • SynQuest Laboratories
  • 2,4,6-Tris(isopropyl)benzenesulfonyl chloride 98.0%
  • 100 g
  • $ 64.00
  • Sigma-Aldrich
  • 2,4,6-Triisopropylbenzenesulfonyl chloride 97%
  • 100g
  • $ 171.00
  • Sigma-Aldrich
  • 2,4,6-Triisopropylbenzenesulfonyl chloride 97%
  • 25g
  • $ 68.40
  • Oakwood
  • 2,4,6-Triisopropylbenzenesulfonyl chloride
  • 100g
  • $ 45.00
  • Oakwood
  • 2,4,6-Triisopropylbenzenesulfonyl chloride 98%
  • 25g
  • $ 14.00
Total 120 raw suppliers
Chemical Property of 2,4,6-Triisopropylbenzenesulfonyl chloride Edit
Chemical Property:
  • Appearance/Colour:White to cream solid 
  • Vapor Pressure:9.55E-05mmHg at 25°C 
  • Melting Point:92-94 °C(lit.) 
  • Refractive Index:1.505 
  • Boiling Point:349.3 °C at 760 mmHg 
  • Flash Point:165.1 °C 
  • PSA:42.52000 
  • Density:1.096 g/cm3 
  • LogP:6.06510 
  • Storage Temp.:Store at RT. 
  • Sensitive.:Moisture Sensitive 
  • Solubility.:ethanol: 50 mg/mL, clear 
  • Water Solubility.:decomposes 
  • XLogP3:5.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:302.1107288
  • Heavy Atom Count:19
  • Complexity:363
Purity/Quality:

98% *data from raw suppliers

2,4,6-Triisopropylbenzenesulfonyl chloride *data from reagent suppliers

Safty Information:
  • Pictogram(s): Corrosive
  • Hazard Codes:
  • Statements: 34-29 
  • Safety Statements: 26-36/37/39-45-27 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC(C)C1=CC(=C(C(=C1)C(C)C)S(=O)(=O)Cl)C(C)C
  • Uses 2,4,6-Triisopropylbenzenesulfonyl chloride is used for the synthesis of glycerophospholipids as a condensing agent and in the analysis of phosphonolipids in egg yolk by HPLC/MS technique. It acts as a coupling reagent for the synthesis of oligonucleotides and as sulfonates of pyrimidine nucleosides. It also serves as a condensing agent in the synthesis of hydrogen-phosphonate diesters. 2,4,6-Triisopropylbenzenesulfonyl chloride can be used in the analysis of phosphonolipids in eggyolk by HPLC/MS technique. It can also be used to synthesize:Dimeric neomycin-neomycin conjugate with a flexible linker, 2,2′-(ethylenedioxy)bis(ethylamine).Coupling reagents for the synthesis of oligonucleotides.Sulfonates of pyrimidine nucleosides. These sulfonates can be displaced by nucleophiles in the presence of palladium-catalysts.
Technology Process of 2,4,6-Triisopropylbenzenesulfonyl chloride

There total 2 articles about 2,4,6-Triisopropylbenzenesulfonyl chloride 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 chlorosulfonic acid; In chloroform; at 0 ℃;
DOI:10.1021/jo971093e
Guidance literature:
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