74973-36-7

Upstream product

• 81226-95-1 1-phenyl-3-(3-hydroxyphenyl)-2-propen-1-one 
• 1774-47-6 trimethylsulfoxonium iodide 
• 81226-95-1 3-hydroxychalcone 

Downstream Products

• 74973-45-8 3-benzoyl-1-(3-hydroxyphenyl)propanol 

Relevant academic research and scientific papers

Substituted cyclopropyl phenoxymethyl phenyl carbamates and their use as fungicides

Compounds with fungicidal properties are presented having the formula wherein m and n are 0 or 1; X is hydrogen, halo, C1-C4) alkyl or alkoxy; Z is (C1-C12) alkyl or haloalkyl; R, R1, R2, R3, and R4 are independently hydrogen, a halogen, lower alkyl, alke

Substituted cyclopropyl phenoxymethyl phenyl carbamates and their use as fungicides

Compounds with fungicidal properties are presented having the formula wherein m and n are 0 or 1; X is hydrogen, halo, (C1-C4)alkyl or alkoxy; Z is (C1-C12) alkyl or haloalkyl; R, R1, R2, R

Benzyloxy substituted aromatics and their use as fungicides and insecticides

Compounds with fungicidal and insecticidal properties having formula STR1 wherein A is N or CH; V is O or NH; m and n are the integers 0 and 1, provided that m+n is 0 or 1; X is independently selected from hydrogen, halo, (C1 -C4)alk

Benzyloxy substituted aromatics and their use as fungicides and insecticides

Compounds with fungicidal and insecticidal properties having formula wherein A is N or CH; V is O or NH; m and n are the integers 0 and 1, provided that m + n is 0 or 1; X is independently selected from hydrogen, halo, (C1-C4)alkyl,

Reactions of Aryl Cyclopropyl Ketones. A New Synthesis of Aryl Tetralones

Aryl cyclopropyl ketones (2) cyclise to 1-tetralones (3) in the presence of a variety of acid catalysts under mild conditions.Open-chain carbinols (4) are also formed.The ratio of (3) to (4) is dependent on the aryl ring substituents.A cationic mechanism is proposed.Cyclopropyl ketones (1) do not react.Stereoelectronic factors involved in the reactivity of the rigig cyclopropyl ketone (12) are discussed.The reactions of selected phenolic cyclopropyl ketones have been investigated as anionic counterparts to the acid-catalysed reactions.No reaction is observed.