HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 70632245, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131710052 | HCID 131710052 | — |
| Product | HCID 70632245 | HCID 70632245 | 85.7% |
Reaction Steps
t-Butyl 3-ethyl-7-(2-thienylacetamido)-3-cephem-4-carboxylate (23 mg) was treated with trifluoracetic acid at room temperature for 1 hour. The excess trifluoroacetic acid was distilled off azeotropically with dry benzene to give the free acid (XVII) as a gum (17 mg) νmax (CHCl3) 1770, 1705, 1680 cm-1The minimum inhibitory concentrations of this compound required to inhibit the growth of five typical Gram-positive bacteria are tabulated below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03939157 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-3e3736a6801048d294173fdd6582123e |
| Source note | uspto-grants-1976_02 |