(CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE

(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

Melting point	120-123 °C (dec.) 120-123 °C (lit.)
storage temp.	2-8°C
Sensitive	Hygroscopic
BRN	3924139
CAS DataBase Reference	17577-28-5(CAS DataBase Reference)
EPA Substance Registry System	Phosphonium, (2-ethoxy-2-oxoethyl)triphenyl-, chloride (17577-28-5)

Safety Information

MSDS Information

(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

(CARBOETHOXYMETHYL)TRIPHENYLPHOSPHONIUM CHLORIDE HYDRATE Preparation Products And Raw materials

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