BENZYL (TRIPHENYLPHOSPHORANYLIDENE)ACETATE

pro_cas
15097-38-8
pro_cdbregno
CCD00091387
pro_formula
C27 H23 O2 P
pro_molWeight
410.451

basic_info

Product_Name: BENZYL (TRIPHENYLPHOSPHORANYLIDENE)ACETATE
CAS: 15097-38-8
EnglishSynonyms: BENZYL 2-(TRIPHENYLPHOSPHORANYLIDENE)ACETATE ; BENZYL (TRIPHENYLPHOSPHORANYLIDENE)ACETATE ; 2-(TRIPHENYLPHOSPHORANYLIDENE)ACETIC ACID PHENYLMETHYL ESTER ; BENZYL 2-(TRIPHENYL-LAMBDA(5)-PHOSPHANYLIDENE)ACETATE ; (BENZYLOXYCARBONYLMETHYLENE)TRIPHENYLPHOSPHORANE
pro_mdlNumber: MFCD00191787
pro_acceptors: 2
pro_donors: 0
pro_smile: c1ccc(cc1)COC(=O)C=P(c2ccccc2)(c3ccccc3)c4ccccc4
InChi: InChI=1S/C27H23O2P/c28-27(29-21-23-13-5-1-6-14-23)22-30(24-15-7-2-8-16-24,25-17-9-3-10-18-25)26-19-11-4-12-20-26/h1-20,22H,21H2
InChiKey: InChIKey=INKMLGJBBDRIQR-UHFFFAOYSA-N

property

MeltingPoint: 120-122 DEG C(LIT)
Comments: APPLICATION: REACTANT FOR: TRIBUTYLPHOSPHINE-MEDIATED VINYLOGOUS WITTIG REACTIONS SYNTHESIS OF 1,2-DIOXANES FOR ANTITRYPANOSOMAL ACTIVITY ORGANOCATALYTIC MICHAEL-TYPE REACTIONS / WITTIG REACTIONS OF PHOSPHORUS YLIDES AND UNSATURATED KETONES STEREOSELECTIVE PHOSPHINE-CATALYZED CYCLOADDITION TO FORM SPIROCYCLOPENTENEOXINDOLES ENANTIOSELECTIVE SYNTHESIS OF PANTOTHENIC ACID PREPARATION OF PHOSPHORUS YLIDES FROM PHOSPHORANES AND ACETIC ANHYDRIDE
UNSPSC: 12352103
WGK: 3

secure_info

secure_wgk_germany: 3

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