(6-Chloropyrazin-2-yl)acetic acid manufacturers
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| | (6-Chloropyrazin-2-yl)acetic acid Basic information | | Application |
| Product Name: | (6-Chloropyrazin-2-yl)acetic acid | | Synonyms: | 2-(6-chloropyrazin-2-yl)acetic acid;6-chloro-2-Pyrazineacetic acid;2-Pyrazineacetic acid, 6-chloro-;(6-CHLOROPYRAZIN-2-YL)ACETIC ACID ISO 9001：2015 REACH;(6-Chloropyrazin-2-yl)acetic acid | | CAS: | 930798-25-7 | | MF: | C6H5ClN2O2 | | MW: | 172.57 | | EINECS: | | | Product Categories: | | | Mol File: | 930798-25-7.mol |  |
| | (6-Chloropyrazin-2-yl)acetic acid Chemical Properties |
| Boiling point | 317.2±37.0 °C(Predicted) | | density | 1.497±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | pka | 3.50±0.10(Predicted) | | Appearance | Light brown to brown Solid | | InChI | InChI=1S/C6H5ClN2O2/c7-5-3-8-2-4(9-5)1-6(10)11/h2-3H,1H2,(H,10,11) | | InChIKey | GKCGKFUOTLQOGO-UHFFFAOYSA-N | | SMILES | C1(CC(O)=O)=NC(Cl)=CN=C1 |
| | (6-Chloropyrazin-2-yl)acetic acid Usage And Synthesis |
| Application | (6-Chloropyrazin-2-yl)acetic acid can be used as an organic synthesis intermediate and a pharmaceutical intermediate, mainly in laboratory research and development processes and chemical and pharmaceutical production processes. | | Synthesis | Step 2: To a 20L three-necked round-bottomed flask was added deionized water (9L) and sodium hydroxide (900g, 22.50 mol, 3.07 eq.) in batches and stirred well. Under stirring, 1,3-diethyl 2-(6-chloropyrazin-2-yl)malonate (2 kg, 1.00 eq., crude) was added slowly and dropwise while the reaction temperature was controlled to be lower than 10°C. The reaction was carried out at a temperature below 10°C. The reaction was carried out at a temperature below 10°C. After completion of the reaction, the mixture was stirred at room temperature overnight and then cooled to 0°C. The pH of the reaction solution was adjusted to 9-10 with 37% hydrochloric acid and subsequently extracted with ethyl acetate (3 x 2 L). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was washed with petroleum ether (1 x 1.5 L) and methyl tert-butyl ether (1 x 1.5 L), dried again with anhydrous sodium sulfate and concentrated under reduced pressure to give 463.6 g (37% yield) of 2-(6-chloropyrazin-2-yl)acetic acid as a yellow solid. | | References | [1] Patent: WO2007/35153, 2007, A1. Location in patent: Page/Page column 4-5
[2] Patent: WO2007/35154, 2007, A1. Location in patent: Page/Page column 28-29
[3] Patent: US2015/31674, 2015, A1. Location in patent: Paragraph 0325; 0322 |
| | (6-Chloropyrazin-2-yl)acetic acid Preparation Products And Raw materials |
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