HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 25168940, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Acetyl-L-Cysteine | HCID 12035 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Product | HCID 25168940 | HCID 25168940 | — |
Reaction Steps
N-acetyl-S-phosphocysteine was synthesized according to the procedure followed by Binkely (1954). N-acetyl cysteine (0.5 g) was dissolved in 8 mL of distilled water in an ice bath. The NAC solution was then treated with 0.2 mL of phosphorus oxychloride and with sodium hydroxide to maintain the basic pH of 11. The resulting white solid was dried and re-dissolved in deuterium oxide for 31P, 13C and 1H NMR analysis. After analysis, the sample was dried, re-suspended in water, and treated with 1 mg (10 units) of alkaline phosphatase, and stirred for 2 hours. The solution was dried and resuspended in deuterium oxide for NMR analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09084803B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-16ed8f4456fd4cfa9a79e9b43f9802be |
| Source note | uspto-grants-2015_07 |