75350-30-0

Upstream product

• 527-69-5 2-furancarbonyl chloride 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 98459-03-1 Furan-2-carboxylic acid 4-{[(E)-4-dodecyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-97-0 Furan-2-carboxylic acid 4-{[(E)-4-propoxy-phenylimino]-methyl}-phenyl ester 
• 98459-01-9 Furan-2-carboxylic acid 4-{[(E)-4-octyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-99-2 Furan-2-carboxylic acid 4-{[(E)-4-hexyloxy-phenylimino]-methyl}-phenyl ester 
• 98459-02-0 Furan-2-carboxylic acid 4-{[(E)-4-nonyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-95-8 Furan-2-carboxylic acid 4-{[(E)-4-methoxy-phenylimino]-methyl}-phenyl ester 
• 98458-96-9 Furan-2-carboxylic acid 4-{[(E)-4-ethoxy-phenylimino]-methyl}-phenyl ester 
• 98459-00-8 Furan-2-carboxylic acid 4-{[(E)-4-heptyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-98-1 Furan-2-carboxylic acid 4-{[(E)-4-pentyloxy-phenylimino]-methyl}-phenyl ester 
• 98459-05-3 Furan-2-carboxylic acid 4-{[(E)-4-hexadecyloxy-phenylimino]-methyl}-phenyl ester 
• 98459-04-2 Furan-2-carboxylic acid 4-{[(E)-4-tetradecyloxy-phenylimino]-methyl}-phenyl ester 

Relevant academic research and scientific papers

Synthesis, characterization, biological activity and molecular docking studies of novel schiff bases derived from thiosemicarbazide: Biochemical and computational approach

In this study, eight new Schiff base derivatives (2a-h) were synthesized and their inhibition activities against Acetylcholinesterase (AChE), Butyrylcholinesterase (BChE), α-Glucosidase and Lactoperoxidase (LPO) were investigated. Structures of the synthe

Synthesis of cholesteryl esters of heterocyclic analogs of cinnamic acid and hetaroyloxycinnamic acids by the Wittig reaction

The reaction of cholesteryl triphenylphosphonioacetate chloride with heterocyclic aldehydes and hetaroyloxyarenecarbaldehydes in the presence of base gave the corresponding cholesteryl esters of substituted propenoic acids possessing liquid crystal proper