40932-67-0

Upstream product

• 5069-26-1 2-methyl-5-phenylthiophene 
• 98-88-4 benzoyl chloride 
• 122-78-1 phenylacetaldehyde 
• 93-91-4 1-phenylbutan-1,3-dione 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 19163-21-4 5-phenylthiophene-2-carboxaldehyde 
• 825-55-8 2-phenylthiophene 

Downstream Products

• 133039-69-7 2-phenyl-naphtho[2,3-b]thiophene 

Relevant academic research and scientific papers

One-Pot Synthesis of 2,3,5-Trisubstituted Thiophenes through Three-Component Assembly of Arylacetaldehydes, Elemental Sulfur, and 1,3-Dicarbonyls

The three-component reaction for the synthesis of 2-arylthiophenes has been developed. Easily available arylacetaldehydes, 1,3-dicarbonyls, and elemental sulfur were directly assembled through cascade condensation/ annulation under base conditions. The pr

Hybrid tetra-aryl ethylene compound, polymer and preparation method and application thereof

The invention discloses a hybrid tetra-aryl ethylene compound. The structure of the hybrid tetra-aryl ethylene compound is as shown in the specification, wherein, Ar1 is phenyl or hexahydric heteroaryl; Ar2 and Ar3 are phenyl, hexahydric heteroaryl or quinary heteroaryl independently and respectively; X is nitrogen, oxygen, sulphur or silicon; R1, R2 and R3 are hydrogen, fluorine, chorine, bromine, iodine, methyl, ethyl, propyl, isopropyl, normal-butyl, isobutyl, tertiary butyl, methoxy, ethyoxyl, amino, hydroxyl, carboxyl, nitryl, sulfonic acid group, trifluoromethyl, phenyl, benzyl, benzoyl, para-bromophenyl, para-fluorophenyl, thiophene, pyridine, or crown ether. The invention further discloses a preparation method of the hybrid tetra-aryl ethylene compound and an application thereof, and discloses a polymer of the hybrid tetra-aryl ethylene compound, a preparation method and an application thereof. The hybrid tetra-aryl ethylene compound is unique in structure performance; the compound has good photochromic performance as well as excellent aggregation-induced emission performance.