139004-93-6 - Names and Identifiers
Name | (R)-Piperidin-2-Ylmethyl-Carbamic Acid Tert-Butyl Ester
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Synonyms | S-2-BOC-AMINOMETHYL-PIPERIDINE-HCl tert-Butyl-methyl(piperidin-2-yl)carbamat tert-Butyl methyl(piperidin-2-yl)carbamate tert-butyl N-methyl-N-(2-piperidyl)carbamate (S)-tert-Butyl (piperidin-2-ylMethyl)carbaMate tert-butyl (S)-(piperidin-2-ylmethyl)carbamate tert-Butyl ((2S)-piperidin-2-ylmethyl)carbamate tert-butyl N-[(2S)-piperidin-2-ylmethyl]carbamate Piperidin-2-ylmethyl-carbamic acid tert-butyl ester (S)-2-[[(tert-Butoxycarbonyl)amino]methyl]piperidine (R)-Piperidin-2-Ylmethyl-Carbamic Acid Tert-Butyl Ester (R)-PIPERIDIN-2-YLMETHYL-CARBAMIC ACID TERT-BUTYL ESTER (S)-tert-butyl piperidin-2-ylmethylcarbamate hydrochloride carbamic acid, N-methyl-N-2-piperidinyl-, 1,1-dimethylethyl ester CarbaMic acid, N-[(2S)-2-piperidinylMethyl]-, 1,1-diMethylethyl ester
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CAS | 139004-96-9 139004-93-6
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InChI | InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13(4)9-7-5-6-8-12-9/h9,12H,5-8H2,1-4H3 |
139004-93-6 - Physico-chemical Properties
Molecular Formula | C11H22N2O2
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Molar Mass | 214.3 |
Density | 1.01g/cm3 |
Boling Point | 287.9°C at 760 mmHg |
Flash Point | 127.9°C |
Vapor Presure | 0.00242mmHg at 25°C |
Appearance | solid |
Storage Condition | 2-8°C |
Refractive Index | 1.485 |
139004-93-6 - Introduction
(S)-tert-butyl (piperidin-2-ylmethyl) carbamate, also known as (S)-tert-butyl(2-piperidylmethyl)carbamate. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
1. appearance: usually white crystal or solid.
2. Melting point: about 67-71°C.
3. molecular formula: C12H23NO2.
4. Molecular weight: 209.32g/mol.
5. solubility: soluble in some organic solvents, such as chloroform, ether, acetonitrile, insoluble in water.
Use:
(S)-tert-butyl (piperidin-2-ylmethyl) carbamate is a chiral reagent commonly used in organic synthesis, which is often used in catalytic reaction and chiral separation in asymmetric synthesis. It can be used as chiral derivatizing agent, catalyst and chiral catalyst etc. Specific applications include drug synthesis, pesticide synthesis, hormone synthesis, etc.
Preparation Method:
The preparation of (S)-tert-butyl (piperidin-2-ylmethyl) carbamate can be carried out by the following method:
1. First, (S)-( )-α-piperidinethoxymethanol and (S)-tert-butylaminazepine were dissolved in dichloromethane, respectively.
2. Then, mix the two solutions, add excess dihydroxyethyl dichloroformate, and the reaction proceeds for a longer time.
3. Finally, an ether solvent was added and distilled to obtain (S)-tert-butyl (piperidin-2-ylmethyl) carbamate.
Safety Information:
1. As a chemical, you need to pay attention to protective measures when using, such as wearing protective gloves and glasses.
2. avoid contact with skin, eyes and mucous membranes, such as accidental contact, should immediately rinse with plenty of water, and seek medical help.
3. in the operation, should avoid the inhalation of dust or steam. Use a protective mask if necessary.
4. The compound should be stored in a dry, dark place, away from fire and oxidant.
Please note that this information is for reference only. Please follow relevant safety procedures and regulations when using this compound.
Last Update:2024-04-09 21:01:54