S-Phthalimidomethyl

S-Trimethylacetamidomethyl, 476 S-Benzamidomethyl, 477 S-Allyloxycarbonylaminomethyl, 477 S-Phenylacetamidomethyl, 477 S-Phthalimidomethyl, 478 S-Acetyl-, S-Carboxy-, and S-Cyanomethyl, 478... 

Chemical Name 0,0-dimethyl S-phthalimidomethyl phosphorodithioate V-dimethoxyphosphino-thioylthiome-thyl)phthalimide 5-[(l,3-dihydro-l,3-dioxo-2/f-isoindol-2-yl)methyl] 0,0-dimethyl phosphorodithioate phospho-rodithioic acid, A-[(l,3-dihydro-l,3-dioxo-2f/-isoindol-2-yl)methyl] 0,0-dimethyl ester Uses nonsystemic acaricide and insecticide. 

SSS 0,0-DIMETHYL S-PHTHALIMIDOMETHYL PHOSPHORODITHIOATE see PHX250 DIMETHYLPOLYSILOXANE see DTR850... 

Dimethylphthalimidiomethyl dithiophosphate 0,0-Dimethyl S-phthalimidomethyl phosphorodithioate. See Phthalimidomethyl-0,0-dimethyl phosphorodithioate 1,4-Dimethylpiperazine. See,N,N -Di methyl piperazine N,N -Dimethylpiperazine CAS 106-58-1... 

Synonyms 0,0-Dimethylphthalimidiomethyl dithiophosphate 0,0-Dimethyl S-phthalimidomethyl phosphorodithioate N-(Mercaptomethyl) phthalimide s-(0,0-dimethyl phosphorodithioate) Phosmet Phosphorodithioic acid, s-((1,3-dihydro-1,3-dioxoisoindol-2-yl) methyl) 0,0-dimethyl ester PMP... 

S-Phthalimidomethyl compounds Dithiocarbamic acid esters from halides... 

It is also important to choose R such that the radical R is able to efficiently reinitiate polymerization. For example, benzyl radical is slow to add to VAc and is therefore also a poor choice for R. RAFT polymerization of VAc and NVP with the S-phthalimidomethyl xanthate 168 gave good control over both molecular weight and dispersity (Table 21). °... 

Sanchez Camazano and Sanchez Martin (72) studied the reaction mechanism and the factors that influence the catalytic hydrolysis of phosmet (o,o-dimethyl-S-(N-phthalimidomethyl)dithiophosphate) by montmorillonite at 30° turated with the... 

Scheme 2 Methods to prepare key intermediate, (S)-2-(phthalimidomethyl) oxirane 19...

Triethylamine and N-chloromethylphthalimide added to a soln. of carbo-benzoxy-L-phenylalanine in dry ethyl acetate, allowed to stand overnight at 37°, then refluxed 15-30 min. phthalimidomethyl carbobenzoxy-L-phenyl-alaninate. Y 70-80%.—No racemization takes place and the esters can be cleaved under mild conditions. F. e. s. G. H. L. Nefkens, Nature 193, 974 (1962). 

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