CERTAIN 1,1-dimethyl-3-phenylureas are potent herbicides1–3. Their herbicidal action is attributed in part to inhibition of chloroplast electron transport (the Hill reaction) in photosynthesis4–7. The corresponding mono-methylureas differ only slightly in herbicidal activity2,8 and in inhibition of the Hill reaction7. Nonmethylated phenylureas are, however, relatively inactive both as herbicides2,9 and Hill inhibitors7. In studies of the relationship between structure, herbicidal activity and inhibition of the Hill reaction, it seemed desirable to prepare and test 4-phenylsemicarbazides with varied methyl substitution in the 1 and 2 positions. The 4-(3,4-dichlorophenyl) analogues shown in Table 1 were chosen as models because of the high herbicidal and Hill inhibitory activities of diuron [I,3-(3,4-dichlorophenyl)-1,1-dimethylurea] and nordiuron [II, 3-(3,4-dichlorophenyl)-1-methylurea].