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| (CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE Basic information |
Product Name: | (CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE | Synonyms: | CARBETHOXYMETHYLTRIPHENYLPHOSPHONIUM CHLORIDE;(CARBOETHOXYMETHYL)-TRIPHENYLPHOSPHONIUMCHLORID;(CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE;(CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE;(ETHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE;(4-ETHOXYCARBONYL)TRIPHENYLPHOSPHONIUM CHLORIDE;(2-ethoxy-2-oxoethyl)triphenylphosphonium chloride;(ETHOXYCARBONYLMETHYL)TRIPHENYLPHOSPHONI UM CHLORIDE, TECH., 80% | CAS: | 17577-28-5 | MF: | C22H22O2P.Cl | MW: | 384.84 | EINECS: | 241-548-2 | Product Categories: | | Mol File: | 17577-28-5.mol | |
| (CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE Chemical Properties |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-36 | WGK Germany | 3 | F | 9 | TSCA | Yes | HS Code | 29319019 |
| (CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE Usage And Synthesis |
Chemical Properties | white to off-white crystals or crystalline powder | Uses | Reactant for:
- Preparation of disubstituted tetrahydrofurans as selective serotonin re-uptake inhibitors for the treatment of depression
- Ring-opening reactions with Wittig reagents
- Enantioselective total synthesis of the phytotoxic lactone herbarumin III via Keck′s asymmetric allylation and Sharpless epoxidation
- Synthesis of fluorobenzofurans via microwave-assisted tandem intramolecular Wittig and Claisen rearrangement reactions
- Preparation of phosphonium derivatives of coumarin
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| (CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE Preparation Products And Raw materials |
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