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| 2,4,6-Triisopropylbenzenesulfonyl chloride Basic information |
Product Name: | 2,4,6-Triisopropylbenzenesulfonyl chloride | Synonyms: | TPSCL 2,4,6-TRIISOPROPYLBENZENESULFONYL HYDRAZIDE;2,4,6-TRIISOPROPYLBENZENESULFONYL CHLORI;2,4,6-Tris(isopropyl)benzenesulphonyl chloride 98+%;2,4,6-Tris(prop-2-yl)benzenesulphonyl chloride;2,4,6-tris(propan-2-yl)benzene-1-sulfonyl chloride;2,4,6-three isopropylbenzene sulfonyl chloride;2,4,6-TRIISOPROPYLBENZENESULFONYL CHLORIDE97%;2,4,6-Triisopropylbenzenesulfonic acid chloride | CAS: | 6553-96-4 | MF: | C15H23ClO2S | MW: | 302.86 | EINECS: | 229-479-6 | Product Categories: | API intermediates;Biochemistry;Condensation & Active Esterification;Condensing Agents (DNA / RNA Synthesis);Nucleosides, Nucleotides & Related Reagents;Protecting Agents, Phosphorylating Agents & Condensing Agents;Sulfur Compounds (for Synthesis);Synthetic Organic Chemistry;Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds;Sulfonyl Halides;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds | Mol File: | 6553-96-4.mol | |
| 2,4,6-Triisopropylbenzenesulfonyl chloride Chemical Properties |
Melting point | 92-94 °C (lit.) | Boiling point | 378C | density | 1.1012 (estimate) | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | solubility | ethanol: 50 mg/mL, clear | form | Crystalline Solid | color | White to slightly beige | Water Solubility | decomposes | Sensitive | Moisture Sensitive | BRN | 1218575 | InChIKey | JAPYIBBSTJFDAK-UHFFFAOYSA-N | CAS DataBase Reference | 6553-96-4(CAS DataBase Reference) |
Hazard Codes | C | Risk Statements | 34-29 | Safety Statements | 26-36/37/39-45-27 | RIDADR | UN 3261 8/PG 2 | WGK Germany | 3 | F | 21 | Hazard Note | Corrosive | HazardClass | 8 | PackingGroup | II | HS Code | 29049020 |
| 2,4,6-Triisopropylbenzenesulfonyl chloride Usage And Synthesis |
Chemical Properties | White to cream solid | 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. | Uses | 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.
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| 2,4,6-Triisopropylbenzenesulfonyl chloride Preparation Products And Raw materials |
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