1-Piperidinecarboxylic acid, 4-mercapto-, 1,1-dimethylethyl ester
tert-butyl 4-sulfanylpiperidine-1-carboxylate
CAS: 134464-79-2
Molecular Formula: C10H19NO2S
1-Piperidinecarboxylic acid, 4-mercapto-, 1,1-dimethylethyl ester - Names and Identifiers
1-Piperidinecarboxylic acid, 4-mercapto-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C10H19NO2S |
| Molar Mass | 217.33 |
| Density | 1.08±0.1 g/cm3(Predicted) |
| Boling Point | 294.2±33.0 °C(Predicted) |
| Flash Point | 131.746°C |
| Vapor Presure | 0.002mmHg at 25°C |
| pKa | 10.52±0.20(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.509 |
| MDL | MFCD10566037 |
1-Piperidinecarboxylic acid, 4-mercapto-, 1,1-dimethylethyl ester - Introduction
1-N-BOC-4-sulfoxypiperidine is an organic compound whose chemical formula is C15H23N3O2. It is a white solid, stable at room temperature. The following is a brief description of the properties, uses, preparation and safety information of the compound:
Nature:
1-N-BOC-4-sulfoxypiperidine is a hydrophobic compound with low solubility. It is soluble in conventional organic solvents and decomposes at higher temperatures. Its melting point is about 76-80 degrees Celsius.
Use:
1-N-BOC-4-sulfoxypiperidine is mainly used as intermediates and reagents in organic synthesis. It is often used in the synthesis of new drug molecules or other organic molecules, and as a protective group in organic synthesis reactions. It has a protective effect on reactive centers such as amino and hydroxyl groups, which can prevent unwanted side reactions during the synthesis.
Preparation Method:
1-N-BOC-4-sulfoxypiperidine is usually synthesized by standard organic synthesis methods. A common method of preparation is the introduction of a BOC protecting group (oxazole formyl) into the 4-mercapto piperidine molecule.
Safety Information:
1-N-BOC-4-sulfoxypiperidine is not currently identified as a particularly harmful or toxic substance. However, it is a chemical substance and should be handled following safe handling and protective measures. When using this compound, follow appropriate laboratory procedures and avoid direct skin contact and inhalation of gases. Should be stored in a dry, cool place, and away from fire and flammable substances.
Nature:
1-N-BOC-4-sulfoxypiperidine is a hydrophobic compound with low solubility. It is soluble in conventional organic solvents and decomposes at higher temperatures. Its melting point is about 76-80 degrees Celsius.
Use:
1-N-BOC-4-sulfoxypiperidine is mainly used as intermediates and reagents in organic synthesis. It is often used in the synthesis of new drug molecules or other organic molecules, and as a protective group in organic synthesis reactions. It has a protective effect on reactive centers such as amino and hydroxyl groups, which can prevent unwanted side reactions during the synthesis.
Preparation Method:
1-N-BOC-4-sulfoxypiperidine is usually synthesized by standard organic synthesis methods. A common method of preparation is the introduction of a BOC protecting group (oxazole formyl) into the 4-mercapto piperidine molecule.
Safety Information:
1-N-BOC-4-sulfoxypiperidine is not currently identified as a particularly harmful or toxic substance. However, it is a chemical substance and should be handled following safe handling and protective measures. When using this compound, follow appropriate laboratory procedures and avoid direct skin contact and inhalation of gases. Should be stored in a dry, cool place, and away from fire and flammable substances.
Last Update：2024-04-10 22:29:15
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View History
1-Piperidinecarboxylic acid, 4-mercapto-, 1,1-dimethylethyl ester
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[(3R)-3-hydroxy-2,2-dimethyl-3-[2-[2-(2-methylpropanoylsulfanyl)ethylcarbamoyl]ethylcarbamoyl]propoxy]phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid
Phosphonic acid, [phenyl(phenylimino)methyl]-, diphenyl ester (9CI)
2-Benzhydryl-2-azaspiro[3.3]heptan-5-ol - B6694
Poly(oxy-1,2-ethanediy), alpha-phosphono-omega-(2,4,6-tris(1-phenylethyl)phenoxy), ca. 20 EO
AC-TYR(PO3H2)-GLU-N(C5H11)2
叔-丁基 4-氰基-4-(3-(环戊氧基)-4-甲氧苯基)哌啶-1-甲酸基酯
Emapalumab
17-Desacetyl Norgestimate-d6 (Major)
4-乙酰丁酸甲酯
[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[(3R)-3-hydroxy-2,2-dimethyl-3-[2-[2-(2-methylpropanoylsulfanyl)ethylcarbamoyl]ethylcarbamoyl]propoxy]phosphoryl]oxy-phosphoryl]oxymethyl]oxolan-3-yl]oxyphosphonic acid
Phosphonic acid, [phenyl(phenylimino)methyl]-, diphenyl ester (9CI)
2-Benzhydryl-2-azaspiro[3.3]heptan-5-ol - B6694
Poly(oxy-1,2-ethanediy), alpha-phosphono-omega-(2,4,6-tris(1-phenylethyl)phenoxy), ca. 20 EO
AC-TYR(PO3H2)-GLU-N(C5H11)2
叔-丁基 4-氰基-4-(3-(环戊氧基)-4-甲氧苯基)哌啶-1-甲酸基酯
Emapalumab
17-Desacetyl Norgestimate-d6 (Major)
4-乙酰丁酸甲酯