HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminophenylboronic acid → 3-Aminophenylboronic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminophenylboronic acid | HCID 92269 | — |
| Reactant | Sulphosuccinimido biotin | HCID 56846292 | — |
| Product | 3-Aminophenylboronic acid | HCID 92269 | — |
| Product | Biotin | HCID 171548 | — |
Reaction Steps
The reaction scheme is illustrated in FIG. 6. FIG. 7 shows IR spectra of the reactants sulfo-NHS-biotin (top) and m-aminophenylboronic acid (middle), and the non-purified reaction mixture after stirring (bottom), comprising the reaction product (i.e. the compound with formula (II)). The bottom spectrum shows an additional vibration at about 1685 cm-1 (indicated with an arrow in FIG. 7) which can be attributed to the amide bond formed between biotin and m-aminophenylboronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097463B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-ec71eaa44c2d4c7abee569f9ce61b65e |
| Source note | uspto-grants-2012_01 |