Diphenic acid
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| Preferred IUPAC name
[1,1′-Biphenyl]-2,2′-dicarboxylic acid | |
| Other names
2,2'-dibenzoic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.006.889 |
| EC Number |
|
| 536420 | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
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| Properties | |
| C14H10O4 | |
| Molar mass | 242.230 g·mol−1 |
| Appearance | white solid |
| Density | 1.2917 g/cm3 |
| Melting point | 235.5 °C (455.9 °F; 508.6 K) |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Diphenic acid, also known as Dibenzoic acid, is an organic compound with the formula (C6H4CO2H)2. It is the most studied of several isomeric dicarboxylic acids of biphenyl. It is a white solid that can be prepared in the laboratory from anthranilic acid via the diazonium salt.[1] It is the product of the microbial action on phenanthrene.[2]
The compound forms a variety of coordination polymers.[3] It also exhibits atropisomerism. It can form an internal anhydride featuring a seven-membered ring fused to the two benzene rings.
