For research use only. Not for therapeutic Use.
(Carbethoxymethylene)triphenylphosphorane(CAT: R009722) is a stabilized Wittig reagent commonly used in organic synthesis for the formation of α,β-unsaturated esters via olefination reactions. Featuring a phosphonium ylide structure with a carbethoxy (ethyl ester) functional group, it enables the selective conversion of aldehydes and ketones into trans-configured α,β-unsaturated compounds. This reagent is especially valuable in constructing carbon–carbon double bonds with high regio- and stereocontrol. It is widely used in the synthesis of complex natural products, pharmaceuticals, and intermediates for fine chemicals. Its bench-stable nature and reliable reactivity make it a key tool in advanced synthetic and medicinal chemistry research.
CAS Number | 1099-45-2 |
Synonyms | 2-(Triphenylphosphoranylidene)acetic Acid Ethyl Ester; (2-Ethoxy-2-oxoethylidene)triphenylphosphorane; Ethyl (triphenylphosphoranylidene)acetate; NSC 72406; |
Molecular Formula | C22H21O2P |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | ethyl 2-(triphenyl-$l^{5} |
InChI | InChI=1S/C22H21O2P/c1-2-24-22(23)18-25(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21/h3-18H,2H2,1H3 |
InChIKey | IIHPVYJPDKJYOU-UHFFFAOYSA-N |
SMILES | CCOC(=O)C=P(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3 |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |