143328-36-3

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 143328-33-0 3-benzyl-3'-formyldiphenylmethane 
• 143328-32-9 3-benzyl-3'-bromodiphenylmethane 
• 143328-31-8 3-benzyl-3'-bromodiphenylmethanol 
• 143328-34-1 3-benzyl-3'-(1-hydroxy-2-propynyl)diphenylmethane 
• 63012-04-4 3-bromobenzhydrol 
• 143328-35-2 1-<3-((3-Benzyl)benzyl)phenyl>prop-2-in-1-on 

Downstream Products

• 143328-37-4 1,3,5-Tris<3-((3-benzoyl)benzoyl)benzoyl>benzol 

Relevant academic research and scientific papers

Exploratory and Mechanistic Studies of the Trimerization Reaction of Benzoylacetylenes in the Presence of Secondary Amine

A variety of benzoylacetylenes are trimerized to give the corresponding 1,3,5-tribenzoylbenzenes when heated with a catalytic amount of diethylamine.A large amount of diethylamine gives γ-(diethylamino)propenoylbenzene at the expense of 1,3,5-tribenzoylbe

APPROACHES TO SUPERPARAMAGNETIC POLYCARBENES AND POLYNITRENES

Poly(m-phenylenemethynyls) and other conjugated polymers to which photolabile diazo or azido groups are attached in every repeating unit have been synthesized.When photolyzed and studied in situ by means of a Faraday balance equipped with a light guide at cryogenic temperatures, the hexa- and nonacarbenes obtained by stepwise synthesis were found to be in S = 6 and 9 ground states, respectively.Attempts to synthesize real polymer samples capable of showing S = 102 ca. 3 were made.These materials would serve as prototypes for organic optomagnetic recording devices.