3741-66-0

Basic information

• Product Name: Ethyl benzoyl carbonate
• Synonyms: Ethyl benzoyl carbonate
• CAS NO: 3741-66-0
• Molecular Weight: 194.187
• Mol File: 3741-66-0.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Ethyl benzoyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl benzoyl carbonate(3741-66-0)
• EPA Substance Registry System: Ethyl benzoyl carbonate(3741-66-0)

Safety Data

• Hazardous Substances Data: 3741-66-0(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 541-41-3 chloroformic acid ethyl ester 
• 65-85-0 benzoic acid 
• 80284-09-9 nitro-carbamic acid ethyl ester; potassium salt 
• 98-88-4 benzoyl chloride 
• 80284-10-2 C₇H₅N₂O₃^(1-)*K⁽¹⁺⁾ 
• 532-32-1 sodium benzoate 

Downstream Products

• 120-51-4 benzoic acid benzyl ester 
• 582-61-6 benzoyl azide 
• 20652-39-5 ethyl diisopropylcarbamate 
• 3553-80-8 ethyl N,N-diethylcarbamate 
• 1696-17-9 N,N-diethylbenzamide 
• 2170-13-0 biphenyl 4-yl benzoate 
• 94-46-2 isoamyl benzoate 
• 5325-94-0 N-Ethoxycarbonylpiperidine 
• 776-75-0 N-benzoylpiperidine 
• 2037-72-1 UR 603 
• 5343-98-6 4-oxo-4-phenylbutanenitrile 
• 1003221-10-0 3-(3-bromophenyl)-5-phenyl-1,2,4-oxadiazole 
• 99430-47-4 N-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)benzamide 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 

Relevant articles and documents

Synthesis and evaluation of α-glucosidase inhibitory activity of sulfonylurea derivatives

Two series of sulfonylureas derivatives including 24 compounds (4, 7, 5a-5o, 8a-8h), among them 17 new derivatives, have been synthesized and evaluated for their α-glucosidase inhibitory activity. Compounds 5c, 5h and 8e showed significant in vitro α-glucosidase inhibition with IC50 values of 5.58, 79.85 and 213.36 μm, respectively, comparing with the standard compounds acarbose (IC50 = 268.29 μm) and glipizide (IC50 = 300.47 μm). The preliminary structure-activity relationships (SARs) of the synthesized compounds were also investigated.

The Synthesis and Characterization of Aromatic Hybrid Anderson-Evans POMs and their Serum Albumin Interactions: The Shift from Polar to Hydrophobic Interactions

Four aromatic hybrid Anderson polyoxomolybdates with Fe3+ or Mn3+ as the central heteroatom have been synthesized by using a pre-functionalization protocol and characterized by using single-crystal X-ray diffraction, FTIR, ESI-MS, s