El Ashry, E. S. H. published the artcileThe scope of the reactions of hydrazines and hydrazones. Part VI. Reaction of hydrazines with dimedone, Computed Properties of 39115-95-2, the publication is Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry (1978), 16B(10), 871-5, database is CAplus.
The reactions of dimedone (I) with hydrazines were studied. I and p-tolylhydrazine gave II (R = NHNHC6H4Me-p), which was deprotonated to give II (R = N:NC6H4Me-p). With excess p-tolylhydrazine, I gave III (Z1 = Z3 = NNHC6H4Me-p, Z2 = O) which was identified as its 2-p-nitrobenzoylhydrazone and III (Z1-Z3 = NNHC6H4Me-p). Reactions of I and II (R = NHNHR1, N:NR1; R1 = Ph, C6H4Me-p) with R2C6H4CONHNH2 (R2 = H, Me, OMe, Cl, Br, I, OH, NO2) gave the corresponding hydrazones. Reaction of I with semicarbazide, thiosemicarbazide and gluconylhydrazines gave the monohydrazones.
Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry published new progress about 39115-95-2. 39115-95-2 belongs to iodides-buliding-blocks, auxiliary class Iodide,Hydrazine,Amine,Benzene,Hydrazide,Amide, name is 4-Iodobenzohydrazide, and the molecular formula is C7H7IN2O, Computed Properties of 39115-95-2.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com