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| | 4-(4-Hydroxyphenyl)benzaldehyde Basic information | | Uses |
| Product Name: | 4-(4-Hydroxyphenyl)benzaldehyde | | Synonyms: | 4-(4-Hydroxyphenyl)benzaldehyde;4'-Hydroxy(1,1'-biphenyl)-4-carboxaldehyde;4-Hydroxy-biphenyl-4'-carboxyaldehyde;4-(4-Formylphenyl)phenol;4'-Hydroxy-biphenyl-4-carboxaldehyde;[1,1'-Biphenyl]-4-carboxaldehyde,4'-hydroxy-;4'-hydroxy-[1,1'-biphenyl]-4-carbaldehyde;4'-Hydroxy-biphenyl-4-carbaldehyde | | CAS: | 100980-82-3 | | MF: | C13H10O2 | | MW: | 198.22 | | EINECS: | | | Product Categories: | | | Mol File: | 100980-82-3.mol |  |
| | 4-(4-Hydroxyphenyl)benzaldehyde Chemical Properties |
| Melting point | 158-161℃ | | Boiling point | 373.7±25.0 °C(Predicted) | | density | 1.202 | | storage temp. | Inert atmosphere,Room Temperature | | pka | 9.57±0.26(Predicted) | | Appearance | Off-white to light yellow Solid |
| | 4-(4-Hydroxyphenyl)benzaldehyde Usage And Synthesis |
| Uses | 4-(4-Formylphenyl)phenol acts as a reagent in the discovery of nonpeptide inhibitors of stromelysin using structure activity relationship by NMR, preparation of nitroimidazole heterocyclic compound and it’s application for treating tuberculosis. | | Uses | 4-(4-Formylphenyl)phenol acts as a reagent in the discovery of nonpeptide inhibitors of stromelysin using structure activity relationship by NMR, preparation of nitroimidazole heterocyclic compound and it’s application for treating tuberculosis. |
| | 4-(4-Hydroxyphenyl)benzaldehyde Preparation Products And Raw materials |
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