Supply 1-Boc-4-piperidone Cas 79099-07-3
Supply 1-Boc-4-piperidone Cas 79099-07-3
Sell 1-Boc-4-piperidone Cas 79099-07-3
Sell 1-Boc-4-piperidone Cas 79099-07-3
4-Piperidone is a derivative of piperidine with the molecular formula C5H9NO. 4-Piperidone is used as an intermediate in the manufacture of chemicals and pharmaceutical drugs. It is a List I chemical in the United States.
1-Boc-4-piperidone is a chemical intermediate used in the synthesis of pharmaceuticals. It is commonly used as a starting material for the preparation of piperidine derivatives, including opioid receptor antagonists and analgesics. This product comes in a 1kg package and should be stored in a cool, dry place away from heat sources or direct sunlight to avoid decomposition. It is important to use appropriate personal protective equipment when handling this compound due to its potential toxicity. The environmental impact of this product is minimal if handled and disposed of properly according to local regulations.
Sell 1-Boc-4-piperidone Cas 79099-07-3
- CAS No.
- 79099-07-3
- Chemical Name:
- N-(tert-Butoxycarbonyl)-4-piperidone
- Synonyms
- TERT-BUTYL 4-OXOPIPERIDINE-1-CARBOXYLATE;1-BOC-4-PIPERIDONE;N-BOC-4-PIPERIDONE;4-OXO-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER;N-BOC-PIPERIDONE;BOC-4-PIPERIDONE;N-BOC-4-PIPERIDINONE;1-BOC-4-PIPERIDINONE;1-BOC-PIPERIDIN-4-ONE;N-tert-butyloxycarbonylpiperidin-4-one
Description | 1-Boc-4-piperidone, also known as Boc-4-piperidone, is a synthetic organic compound used in various scientific and medical research applications. It is a substituted piperidine derivative with a Boc (tert-butoxycarbonyl) group at the 1-position. The compound is widely used in organic synthesis due to its ease of handling and storage. It is also used as a starting material in the synthesis of various organic compounds, such as peptides, amino acids, and other biologically active compounds. |
Synthesis Method | 1-1-Boc-4-piperidonedone can be synthesized from 4-piperidone and tert-butyl bromoacetate in the presence of a base, such as sodium hydroxide. The reaction is typically carried out in an aqueous solution, and the product is isolated by either evaporation or extraction. The product can also be purified by recrystallization from a suitable solvent. |
Synthesis Method Details | Design of the Synthesis Pathway The synthesis of 1-Boc-4-piperidone can be achieved through a series of chemical reactions starting from commercially available starting materials.Starting Materials 4-piperidone, Di-tert-butyl dicarbonate (Boc2O), Triethylamine (TEA), Methanol (MeOH), Sodium hydroxide (NaOH), Hydrochloric acid (HCl), Ethyl acetate (EtOAc), Sodium chloride (NaCl), Anhydrous magnesium sulfate (MgSO4)Reaction Step 1: Protection of 4-piperidone with Boc2O 4-piperidone + Boc2O + TEA -> 1-Boc-4-piperidone Step 2: Hydrolysis of Boc group 1-Boc-4-piperidone + HCl (aq) -> 4-piperidone hydrochloride + Boc2O Step 3: Preparation of 1-Boc-4-piperidone 1-Boc-4-piperidone + NaOH (aq) -> 4-piperidone + NaBoc + H2O Step 4: Extraction of 1-Boc-4-piperidone 4-piperidone + EtOAc + NaCl + H2O -> Organic layer Step 5: Drying of organic layer Organic layer + MgSO4 -> 1-Boc-4-piperidone |
Scientific Research Applications | 1-1-Boc-4-piperidonedone is widely used in scientific research, particularly in in vivo and in vitro studies. It is used as a starting material for the synthesis of various biologically active compounds, such as peptides, amino acids, and other organic molecules. In addition, it is used as a reagent in the synthesis of various pharmaceuticals, such as analgesics and anti-inflammatory drugs. |
Mechanism of Action | 1-1-Boc-4-piperidonedone is believed to act as a substrate for various enzymes in the body, such as proteases and peptidases. It is also believed to act as an inhibitor of various enzymes, such as proteases and peptidases. |
Biochemical and Physiological Effects | 1-1-Boc-4-piperidonedone has been shown to have various biochemical and physiological effects, such as the inhibition of various enzymes, the modulation of various hormones, and the modulation of various neurotransmitters. It has also been shown to have various effects on the cardiovascular system, such as the modulation of blood pressure and heart rate. |
In vivo studies | 1-1-Boc-4-piperidonedone has been used in various in vivo studies, such as to study the effects of various drugs on the body. It has also been used in studies to investigate the effects of various compounds on the central nervous system, as well as to study the effects of various drugs on the immune system. |
In vitro studies | 1-1-Boc-4-piperidonedone has also been used in various in vitro studies, such as to study the effects of various compounds on cell cultures. It has been used to study the effects of various drugs on cell proliferation, as well as to study the effects of various compounds on enzyme activity. |
Biological Activity | 1-1-Boc-4-piperidonedone has been shown to have various biological activities, such as anti-inflammatory, anti-viral, and anti-bacterial activities. It has also been shown to have various pharmacological effects, such as analgesic, anti-convulsant, and anti-depressant effects. |
Advantages and Limitations for Lab Experiments | 1-1-Boc-4-piperidonedone has several advantages for use in laboratory experiments. It is relatively easy to synthesize and handle, and it is relatively stable in aqueous solutions. It is also relatively non-toxic, making it safe to use in laboratory experiments. However, it is not suitable for use in in vivo studies due to its low bioavailability. |
Pharmacodynamics | 1-1-Boc-4-piperidonedone has been shown to have various pharmacodynamic effects, such as the inhibition of various enzymes, the modulation of various hormones, and the modulation of various neurotransmitters. It has also been shown to have various effects on the cardiovascular system, such as the modulation of blood pressure and heart rate. |
Future Directions | 1-1-Boc-4-piperidonedone has many potential future applications in scientific research. It could be used in the synthesis of various biologically active compounds, such as peptides, amino acids, and other organic molecules. It could also be used in the synthesis of various pharmaceuticals, such as analgesics and anti-inflammatory drugs. In addition, it could be used in studies to investigate the effects of various compounds on the central nervous system and the immune system. Additionally, it could be used in studies to investigate the effects of various compounds on cell cultures and enzyme activity. Finally, it could be used in studies to investigate the effects of various compounds on the cardiovascular system, such as the modulation of blood pressure and heart rate. |
CAS RN | 79099-07-3 |
Product Name | 1-Boc-4-piperidone |
Molecular Formula | C10H17NO3 |
Molecular Weight | 199.25 g/mol |
IUPAC Name | tert-butyl 4-oxopiperidine-1-carboxylate |
InChI | InChI=1S/C10H17NO3/c1-10(2,3)14-9(13)11-6-4-8(12)5-7-11/h4-7H2,1-3H3 |
InChI Key | ROUYFJUVMYHXFJ-UHFFFAOYSA-N |
SMILES | CC(C)(C)OC(=O)N1CCC(=O)CC1 |
Canonical SMILES | CC(C)(C)OC(=O)N1CCC(=O)CC1 |
Other CAS RN | 79099-07-3 |
Pictograms | Irritant |
Synonyms | 4-Oxo-1-piperidinecarboxylic Acid 1,1-Dimethylethyl Ester; 1,1-Dimethylethyl 4-Oxo-1-piperidinecarboxylate; 1-(tert-Butoxycarbonyl)-4-oxopiperidine; |
Origin of Product | china |
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