51112-81-3

Basic information

• Product Name: endoxo-delta(4)-tetrahydrophthalic acid
• Synonyms: endoxo-delta(4)-tetrahydrophthalic acid
• CAS NO: 51112-81-3
• Molecular Formula: C₈H₈O₅
• Molecular Weight: 184.14612
• Mol File: 51112-81-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 464.5°Cat760mmHg
• Flash Point: 199.1°C
• Appearance: /
• Density: 1.614g/cm³
• PKA: 3.53±0.40(Predicted)
• CAS DataBase Reference: endoxo-delta(4)-tetrahydrophthalic acid(CAS DataBase Reference)
• NIST Chemistry Reference: endoxo-delta(4)-tetrahydrophthalic acid(51112-81-3)
• EPA Substance Registry System: endoxo-delta(4)-tetrahydrophthalic acid(51112-81-3)

Safety Data

• Hazardous Substances Data: 51112-81-3(Hazardous Substances Data)

Upstream product

• 110-00-9 furan 
• 110-16-7 maleic acid 
• 81486-09-1 (2-endo,3-exo)-7-oxabicyclo<2.2.1>hept-5-ene-2,3-bis(carbonyl chloride) 
• 108-31-6 maleic anhydride 
• 7440-44-0 pyrographite 
• 7732-18-5 water 
• 28871-62-7 7-Oxa-bicyclo-<2.2.1>-hept-5-en-2,3-exo,exo-dicarbonsaeure 

Downstream Products

• 55423-53-5 (2-endo,3-exo)-7-oxabicyclo<2.2.1>heptane-2,3-dimethanol 
• 97909-51-8 (2-endo,3-exo)-7-oxabicyclo<2.2.1>heptane-2,3-dimethanol bis(4-methylbenzenesulfonate) 
• 28871-63-8 endo-7-oxabicyclo<2.2.1>heptane-2,3-dicarboxylic acid 
• 145-73-3 (+)-7-Oxanorbornan-trans-2,3-dicarbonsaeure 
• 96410-99-0 (1S,2S,6S,7R)-3-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-4,10-dioxa-tricyclo[5.2.1.0^2,6]decane 
• 96410-99-0 (1R,2R,6R,7S)-3-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-4,10-dioxa-tricyclo[5.2.1.0^2,6]decane 
• 51112-82-4 endo-3a,4,7,7a-tetrahydro-4,7-epoxyisobenzofuran-1-(3H)-one 
• 6253-21-0 endo-hexahydro-4,7-epoxyisobenzofuran-1(3H)-one 
• 96411-00-6 [3aS-(3aα,4α,7α,7aα)]-Octahydro-1-benzyloxy-4,7-epoxyisobenzofuran 

Relevant articles and documents

Supramolecular chemistry under mechanochemical conditions: A small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction

We describe the integration of a small-molecule hydrogen-bond-donor template into a cascade reaction that is comprised of a combination of molecular and supramolecular events. The cascade is performed mechanochemically and in the presence of μL amounts of

Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function

Fused cyclic compounds, methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders, and pharmaceutical compositions containing such compounds.

Synthesis and in vitro pharmacology of 7-oxabicyclo[2.2.1]heptane analogues of thromboxane A2/PGH2

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