- Ethyl pipecolinate
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- $0.00 / 1kg
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2025-06-20
- CAS:15862-72-3
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 100tons
- Ethyl pipecolinate
-
- $10.00 / 1kg
-
2023-11-03
- CAS:15862-72-3
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 100tons
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| | Ethyl pipecolinate Basic information |
| Product Name: | Ethyl pipecolinate | | Synonyms: | (2R)-2-piperidin-1-iumcarboxylic acid ethyl ester;2-ETHYL PIPECOLINICTATE 98.5+%;2-CARBETHOXY PIPERIDINE;Ethyl nipecotate(ethyl 2-Piperidinecarboxylate);Ethyl pipecolinate, 98+%;Ethyl DL-piperidine-2-carboxylate hydrochloride;Ethyl Pipecolate;(±)-Ethyl piperidine-2-carboxylate, DL-Homoproline ethyl ester | | CAS: | 15862-72-3 | | MF: | C8H15NO2 | | MW: | 157.21 | | EINECS: | 239-990-6 | | Product Categories: | Piperidine | | Mol File: | 15862-72-3.mol |  |
| | Ethyl pipecolinate Chemical Properties |
| Boiling point | 216-217 °C (lit.) | | density | 1.006 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.456 | | Fp | 115 °F | | storage temp. | 2-8°C | | pka | 8.40±0.10(Predicted) | | form | Liquid | | color | Clear colorless to light yellow | | BRN | 81694 | | InChI | 1S/C8H15NO2/c1-2-11-8(10)7-5-3-4-6-9-7/h7,9H,2-6H2,1H3 | | InChIKey | SZIKRGHFZTYTIT-UHFFFAOYSA-N | | SMILES | CCOC(=O)C1CCCCN1 | | CAS DataBase Reference | 15862-72-3(CAS DataBase Reference) | | NIST Chemistry Reference | Ethyl pipecolinate(15862-72-3) |
| Hazard Codes | Xi,C | | Risk Statements | 10-36/37/38-34-20/21 | | Safety Statements | 26-36-36/37/39 | | RIDADR | UN 1993 3/PG 3 | | WGK Germany | 3 | | F | 10 | | Hazard Note | Irritant | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29333990 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Eye Irrit. 2 Flam. Liq. 3 Skin Irrit. 2 STOT SE 3 |
| | Ethyl pipecolinate Usage And Synthesis |
| Chemical Properties | clear colorless to light yellow liquid | | Uses | Reactant for: Combinatorial chemistry with hydrazones Swift hydroamination Synthesis of HCV NS5B polymerase inhibitors Preparation of selective androgen receptor modulators Decarbonylative arylation at sp3 carbon centers Synthesis of quinoline derivatives as selective a2C-adrenoceptor antagonists |
| | Ethyl pipecolinate Preparation Products And Raw materials |
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