113202-49-6

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 34743-88-9 2-(4-bromophenoxy)ethanol 

Downstream Products

• 113202-50-9 1,2-diphenyl-1-<4-(2-hydroxyethoxy)phenyl>-ethylene 
• 113202-59-8 1,2-diphenyl-2-iodo-1-<4-(2-methanesulfonyloxyethoxy)phenyl>ethylene 
• 113202-57-6 1-<4-(2-t-butyldimethylsilyloxyethoxy)phenyl>-1,2-diphenyl-2-iodoethylene 
• 113202-52-1 2-bromo-1-<4-(2-t-butyldimethylsilyloxyethoxy)phenyl>-1,2-diphenylethylene 
• 113202-47-4 1-<4-(2-N-aziridylethoxy)phenyl>-1,2-diphenyl-2-iodoethylene 
• 113202-51-0 1-<4-(2-t-butyldimethylsilyloxyethoxy)phenyl>-1,2-diphenylethylene 
• 113202-58-7 1,2-diphenyl-1-<4-(2-hydroxyethoxy)phenyl>-2-iodoethylene 

Relevant academic research and scientific papers

PHOTOBASE GENERATOR

Provided are a photobase generator having higher sensitivity to light than do conventional photobase generators, and a photosensitive resin composition containing the photobase generator. The present invention is a photobase generator characterized in containing a salt represented by general formula (1). (In formula (1), R 1 -R 4 are mutually independent groups represented by general formula (2), C1-18 alkyl groups, or Ar, with at least one being a group represented by general formula (2); in formula (2), (D) is a divalent group bonded on at least one side to elemental boron, and Ar 1 is the same as the aforementioned Ar; and Q + is a monovalent onium cation.) €?€?€?€?€?€?€?€?-(D)-Ar 1 €?€?€?€?€?(2)

[125I]Iododesethyl tamoxifen aziridine: Synthesis and covalent labeling of the estrogen receptor with an iodine-labeled affinity label

Iododesethyl tamoxifen aziridine (I-Tam-Az), an analog of the estrogen receptor-affinity label tamoxifen aziridine (Tam-Az) in which the ethyl group has been replaced by an iodine, has been prepared by two routes: (a) metallation of a bromotriarylethylene