7-ACA

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7-Aminocephalosporanic acid
Partially condensed, stereo, skeletal formula of 7-aminocephalosporanic acid
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Names
Systematic IUPAC name
3-(Acetyloxymethyl)-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Other names
7-Aminocephalosporinic acid
Identifiers
957-68-6 YesY
3DMet B02139
Abbreviations 7-ACA
622637, 8919572
ChEBI CHEBI:2255 N
ChEMBL ChEMBL1161449 N
ChemSpider 390087 YesY
EC Number 213-485-0
Jmol 3D model Interactive image
KEGG C07756 N
MeSH 7-Aminocephalosporanic+acid
PubChem 483168
  • InChI=1S/C10H12N2O5S/c1-4(13)17-2-5-3-18-9-6(11)8(14)12(9)7(5)10(15)16/h6,9H,2-3,11H2,1H3,(H,15,16)/t6-,9-/m1/s1 YesY
    Key: HSHGZXNAXBPPDL-HZGVNTEJSA-N YesY
  • O=C2N1/C(=C(\CS[C@@H]1[C@@H]2N)COC(=O)C)C(=O)O
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).
N verify (what is YesYN ?)
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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