7-ACA
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Template:Chembox image cellTemplate:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox headerbarTemplate:Chembox GHS (set)Template:Chembox Datapage checkTemplate:Chembox Footer| Template:Longitem | Template:Unbulleted list |
| Abbreviations | 7-ACA |
| Template:Longitem | 622637, 8919572 |
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| EC Number | Template:Unbulleted list |
| KEGG | Template:Unbulleted list |
| MeSH | 7-Aminocephalosporanic+acid |
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| Molar mass | Template:Chem molar mass |
| Melting point | Template:Chembox CalcTemperatures |
| log P | −1.87 |
| Acidity (pKa) | 2.59 |
| Basicity (pKb) | 11.41 |
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7-ACA (7-aminocephalosporanic acid) is the core chemical structure (a synthon) for the synthesis of cephalosporin antibiotics and intermediates. It can be obtained by chemoenzymatic hydrolysis of cephalosporin C.[1][2]
The production of 7-ACA (7-aminocephalosporanic acid) is predominantly segmented into two methods which is Enzymatic Hydrolysis and Chemical Cracking. These processes are essential for the synthesis of various cephalosporin antibiotics.[3]
See also
References
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