tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate
(S)-1-N-BOC-PIPERIDINE-2-ETHANOL
CAS: 199942-74-0
Molecular Formula: C12H23NO3
tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate - Names and Identifiers
| Name | (S)-1-N-BOC-PIPERIDINE-2-ETHANOL |
| Synonyms | (S)-1-N-BOC-PIPERIDINE-2-ETHANOL tert-butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate 1-Piperidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, (2S)- 1-Piperidinecarboxylic acid, 2-(2-hydroxyethyl)-, 1,1-dimethylethyl ester, (2S) |
| CAS | 199942-74-0 |
| InChI | InChI=1/C12H23NO3/c1-12(2,3)16-11(15)13-8-5-4-6-10(13)7-9-14/h10,14H,4-9H2,1-3H3/t10-/m0/s1 |
tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate - Physico-chemical Properties
| Molecular Formula | C12H23NO3 |
| Molar Mass | 229.32 |
| Density | 1.043 |
| Boling Point | 324.1±15.0 °C(Predicted) |
| Flash Point | 149.8°C |
| Vapor Presure | 1.97E-05mmHg at 25°C |
| pKa | 15.15±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.478 |
tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate - Introduction
(S)-I is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
(S)-is a white crystalline solid with a chemical formula of C13H23NO3 and a molecular weight of 241.33g/mol. It has good solubility and can be dissolved in some organic solvents.
Use:
(S)-can be used as an intermediate in organic synthesis. It can be used to synthesize biologically active compounds such as drugs, pesticides and biomarkers. Its unique structure and chemical properties make it widely used in the synthesis of organic compounds.
Method:
The preparation method of (S)-is to react piperidine and (Boc)2O under appropriate reaction conditions. The reaction is carried out by first dissolving the piperidine in a suitable solvent and then adding (Boc)2O. After completion of the reaction, the product is obtained through the steps of crystallization, filtration and drying.
Safety Information:
There are no specific reports on the safety information of (S)-(S)-(S). However, as an organic compound, it may be toxic to the human body, so it is necessary to take appropriate safety measures during handling and storage, such as wearing protective gloves, glasses and protective clothing. At the same time, it needs to be operated in a well-ventilated environment to avoid inhaling its vapors or contacting the skin. If necessary, the operation should be carried out under professional guidance.
Nature:
(S)-is a white crystalline solid with a chemical formula of C13H23NO3 and a molecular weight of 241.33g/mol. It has good solubility and can be dissolved in some organic solvents.
Use:
(S)-can be used as an intermediate in organic synthesis. It can be used to synthesize biologically active compounds such as drugs, pesticides and biomarkers. Its unique structure and chemical properties make it widely used in the synthesis of organic compounds.
Method:
The preparation method of (S)-is to react piperidine and (Boc)2O under appropriate reaction conditions. The reaction is carried out by first dissolving the piperidine in a suitable solvent and then adding (Boc)2O. After completion of the reaction, the product is obtained through the steps of crystallization, filtration and drying.
Safety Information:
There are no specific reports on the safety information of (S)-(S)-(S). However, as an organic compound, it may be toxic to the human body, so it is necessary to take appropriate safety measures during handling and storage, such as wearing protective gloves, glasses and protective clothing. At the same time, it needs to be operated in a well-ventilated environment to avoid inhaling its vapors or contacting the skin. If necessary, the operation should be carried out under professional guidance.
Last Update：2024-04-09 21:54:55
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Product Name: (S)-1-N-BOC-PIPERIDINE-2-ETHANOL Visit Supplier Webpage Request for quotation
CAS: 199942-74-0
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View History
tert-Butyl (2S)-2-(2-hydroxyethyl)piperidine-1-carboxylate
2-(氨甲基)-1H苯并[d]咪唑-6-羧酸盐酸盐
1-(6-乙氧基-2-甲硫基-嘧啶-4-基)-哌啶-4-基胺盐酸盐
4-Heptanone, 1,7-bis[bis(1-methylethyl)amino]-3,5-diphenyl-3,5-di-2-pyridinyl-
1-[2-fluoro-6-(2-methoxy-4-methylphenoxy)phenyl]ethan-1-amine
Ropinirole Related Compound A (50 mg) (4-(2-hydroxyethyl)indolin-2-one)
2-(氨甲基)-1H苯并[d]咪唑-6-羧酸盐酸盐
1-(6-乙氧基-2-甲硫基-嘧啶-4-基)-哌啶-4-基胺盐酸盐
4-Heptanone, 1,7-bis[bis(1-methylethyl)amino]-3,5-diphenyl-3,5-di-2-pyridinyl-
1-[2-fluoro-6-(2-methoxy-4-methylphenoxy)phenyl]ethan-1-amine
Ropinirole Related Compound A (50 mg) (4-(2-hydroxyethyl)indolin-2-one)