7-ACA
From Infogalactic: the planetary knowledge core
Partially condensed, stereo, skeletal formula of 7-aminocephalosporanic acid | |
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Names | |
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Systematic IUPAC name
3-(Acetyloxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
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Other names
7-Aminocephalosporinic acid
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Identifiers | |
957-68-6 ![]() |
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3DMet | B02139 |
Abbreviations | 7-ACA |
622637, 8919572 | |
ChEBI | CHEBI:2255 ![]() |
ChEMBL | ChEMBL1161449 ![]() |
ChemSpider | 390087 ![]() |
EC Number | 213-485-0 |
Jmol 3D model | Interactive image |
KEGG | C07756 ![]() |
MeSH | 7-Aminocephalosporanic+acid |
PubChem | 483168 |
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Properties | |
C10H12N2O5S | |
Molar mass | 272.27 g·mol−1 |
Melting point | 300 °C (572 °F; 573 K)[1] |
log P | -1.87 |
Acidity (pKa) | 2.59 |
Basicity (pKb) | 11.41 |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
7-ACA (7-aminocephalosporanic acid) is the core chemical structure for the synthesis of cephalosporin antibiotics and intermediates. It can be obtained by chemoenzymatic hydrolysis of cephalosporin C.[2][3]
See also
References
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- ↑ 7-ACA at Chemblink
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