75350-30-0

Basic information

• Product Name: 4-FORMYLPHENYL 2-FUROATE
• Synonyms: ART-CHEM-BB B014264;AKOS B014264;4-FORMYLPHENYL 2-FUROATE;(4-formylphenyl) furan-2-carboxylate;(4-methanoylphenyl) furan-2-carboxylate;2-furancarboxylic acid (4-formylphenyl) ester;A2437/0103278;CBDivE_001469
• CAS NO: 75350-30-0
• Molecular Formula: C₁₂H₈O₄
• Molecular Weight: 216.19
• Mol File: 75350-30-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 95 °C(Solv: ethanol (64-17-5))
• Boiling Point: 360.8±22.0 °C(Predicted)
• Appearance: /
• Density: 1.292±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 4-FORMYLPHENYL 2-FUROATE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-FORMYLPHENYL 2-FUROATE(75350-30-0)
• EPA Substance Registry System: 4-FORMYLPHENYL 2-FUROATE(75350-30-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 75350-30-0(Hazardous Substances Data)

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 
• 98458-96-9 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 
• 98458-99-2 Furan-2-carboxylic acid 4-{[(E)-4-hexyloxy-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 
• 98458-95-8 Furan-2-carboxylic acid 4-{[(E)-4-methoxy-phenylimino]-methyl}-phenyl ester 
• 98459-02-0 Furan-2-carboxylic acid 4-{[(E)-4-nonyloxy-phenylimino]-methyl}-phenyl ester 
• 98459-01-9 Furan-2-carboxylic acid 4-{[(E)-4-octyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-98-1 Furan-2-carboxylic acid 4-{[(E)-4-pentyloxy-phenylimino]-methyl}-phenyl ester 
• 98458-97-0 Furan-2-carboxylic acid 4-{[(E)-4-propoxy-phenylimino]-methyl}-phenyl ester 

Relevant articles and documents

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