5248-12-4

Basic information

• Product Name: anti head-to-head coumarin dimer
• Synonyms: anti head-to-head coumarin dimer
• CAS NO: 5248-12-4
• Molecular Weight: 292.291
• Mol File: 5248-12-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: anti head-to-head coumarin dimer(CAS DataBase Reference)
• NIST Chemistry Reference: anti head-to-head coumarin dimer(5248-12-4)
• EPA Substance Registry System: anti head-to-head coumarin dimer(5248-12-4)

Safety Data

• Hazardous Substances Data: 5248-12-4(Hazardous Substances Data)

Upstream product

• 85381-11-9 2-ethoxycarbonyl-1-(2-hydroxyphenyl)-1α,2α,2aβ,8bβ-tetrahydro-3H-cyclobutachromen-3-one 
• 85381-12-0 2-butylcarbamoyl-1-(2-hydroxyphenyl)-1α,2α,2aβ,8bβ-tetrahydro-3H-cyclobutachromen-3-one 
• 85381-13-1 1-(2-hydroxyphenyl)-2-phenylcarbamoyl-1α,2α,2aβ,8bβ-tetrahydro-3H-cyclobutachromen-3-one 
• 835652-06-7 diethyl t-3,c-4-bis(2-hydroxyphenyl)-r-1,t-2-cyclobutanedicarboxylate 
• 102680-52-4 t-3,c-4-bis(2-hydroxyphenyl)-r-1,t-2-cyclobutanedianilide 

Downstream Products

• 85381-12-0 2-butylcarbamoyl-1-(2-hydroxyphenyl)-1-α,2α,2aβ,8bβ-tetrahydro-3H-cyclobuta--chromen-3-one 
• 7734-65-8 t-3,c-4-bis(2-hydroxyphenyl)-r-1,t-2-cyclobutanedicarboxylic acid 
• 211253-49-5 [(1S,2S,3S,4S)-2-Hydroxymethyl-3,4-bis-(2-methoxy-phenyl)-cyclobutyl]-methanol 
• 110350-35-1 3,4-bis(2-methoxyphenyl)-1,2-cyclobutanedicarbonyl dichloride 
• 110456-57-0 3,4-bis(2-methoxyphenyl)-1,2-cyclobutanedicarboxylic acid 
• 867273-36-7 (1S,2S,3S,4S)-3,4-Bis-(2-methoxy-phenyl)-cyclobutane-1,2-dicarboxylic acid diamide 
• 867273-40-3 C₂₀H₂₂N₆O₂ 
• 867273-41-4 C-[(1S,2S,3S,4S)-2-Aminomethyl-3,4-bis-(2-methoxy-phenyl)-cyclobutyl]-methylamine 

Relevant articles and documents

Thermal Behavior of Head-to-head Coumarin Dimers and Their Lactone-opened Derivatives

The thermal behavior of head-to-head coumarin dimers and twelwe lactone-opened derivatives was investigated.Though the lactone rings in coumarin dimers are very susceptible to nucleophilic ring-opening, heating these derivatives reformed six-membered lactone rings except for certain imide and diamide derivatives.The large neiboring group effect allowed the relactonization by the attack of hydroxyphenyl group to carbonyl carbon in preference to the scission of cyclobutane ring.