313471-11-3

Basic information

• Product Name: ethyl 2-((6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy)acetate
• Synonyms: ethyl 2-((6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy)acetate
• CAS NO: 313471-11-3
• Molecular Formula: C₁₇H₁₈O₅
• Molecular Weight: 302.32182
• Mol File: 313471-11-3.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 477.4±45.0 °C(Predicted)
• Appearance: /
• Density: 1.27±0.1 g/cm3(Predicted)
• CAS DataBase Reference: ethyl 2-((6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-((6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy)acetate(313471-11-3)
• EPA Substance Registry System: ethyl 2-((6-oxo-7,8,9,10-tetrahydro-6H-benzo[c]chromen-3-yl)oxy)acetate(313471-11-3)

Safety Data

• Hazardous Substances Data: 313471-11-3(Hazardous Substances Data)

Upstream product

• 3722-44-9 3-hydroxy-7,8,9,10-tetrahydrobenzo[c]chromen-6-one 
• 105-36-2 ethyl bromoacetate 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 108-46-3 recorcinol 
• 105-39-5 chloroacetic acid ethyl ester 
• 1139-83-9 urolithin B 

Downstream Products

• 325737-63-1 2-[(7,8,9,10-tetrahydro-6-oxo-6H-dibenzo[b,d]pyran-3-yl)oxy]acetic acid 

Relevant articles and documents

Modified coumarins. 5. Amino-acid derivatives of 3-hydroxy-7,8,9,10-tetrahydrobenzo[c]chromen-6-one

Peptide-chemistry methods (symmetric anhydrides and activated esters) and the Mannich reaction were used to prepare various conjugates of amino acids with 7,8,9,10-tetrahydrobenzo[c]chromen-6-one in which the amino acids are bound to the coumarin by the C- or N-terminus.

Design, synthesis, and biological evaluation of new urolithin amides as multitarget agents against Alzheimer's disease

A series of urolithin amide (i.e., URO-4–URO-10 and THU-4–THU-10) derivatives was designed and synthesized, and their chemical structures were confirmed with spectroscopic techniques and elemental analysis. The title compounds and synthesis intermediates