HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → Anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| Reactant | 1-Amino-2-carboxy-4-(3'-amino-4'-sulfophenylthio)anthraquinone | HCID 14876418 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
Example 21 was repeated, except that the compounds shown in 1st, 2nd and 3rd columns of the following table were used in place of the 1-amino-2-carboxy-4-(3'-amino-4'-sulfophenylthio)anthraquinone, cyanuric chloride and 3-aminobenzenesulfonic acid, respectively, thereby obtaining a corresponding anthraquinone compound. The color shade on cotton of the compound is as shown in a 4th column of the table.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05266696 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-cc826c52970b4beaa6bf321e7b21d674 |
| Source note | uspto-grants-1993_11 |