Hexanoic acid, 3,5,5-trimethyl-, 2,2,6,6-tetramethyl-1-[2-[(3,5,5-trimethyl-1-oxohexyl)oxy]ethyl]-4-piperidinyl ester
2,2,6,6-tetramethyl-1-{2-[(3,5,5-trimethylhexanoyl)oxy]ethyl}piperidin-4-yl 3,5,5-trimethylhexanoate
CAS: 1445870-18-7
Molecular Formula: C29H55NO4
Hexanoic acid, 3,5,5-trimethyl-, 2,2,6,6-tetramethyl-1-[2-[(3,5,5-trimethyl-1-oxohexyl)oxy]ethyl]-4-piperidinyl ester - Names and Identifiers
Hexanoic acid, 3,5,5-trimethyl-, 2,2,6,6-tetramethyl-1-[2-[(3,5,5-trimethyl-1-oxohexyl)oxy]ethyl]-4-piperidinyl ester - Physico-chemical Properties
| Molecular Formula | C29H55NO4 |
| Molar Mass | 481.75 |
| Density | 0.947g/cm3 at 20℃ |
| Boling Point | 509.3±45.0 °C(Predicted) |
| Vapor Presure | 0Pa at 25℃ |
| Appearance | Viscous |
| pKa | 8.40±0.10(Predicted) |
Hexanoic acid, 3,5,5-trimethyl-, 2,2,6,6-tetramethyl-1-[2-[(3,5,5-trimethyl-1-oxohexyl)oxy]ethyl]-4-piperidinyl ester - Introduction
2,2, 6,6-Tetramethyl -1-{2-[(3,5, 5-trimethylhexanoyloxy) ethyl] piperidin-4-yl} 3,5,5-Trimethylhexanoate is an organic compound commonly referred to as TMH.
Nature:
TMH is a colorless to pale yellow liquid with low volatility. It has low solubility, being insoluble in water, but soluble in organic solvents such as alcohols and ethers. It is a stable compound that is not easily decomposed and oxidized under regular experimental conditions.
Use:
TMH is a common organic synthesis intermediate. It is commonly used as a functional group protecting agent and reaction intermediate in organic synthesis. Its main use is in the synthesis of pharmaceutical compounds and specific chemicals such as pesticides. In addition, TMH can also be used as an additive to some polymer materials to improve the performance of the material.
Preparation Method:
The preparation methods of TMH are varied, and the most commonly used method is synthesis by chemical synthesis. A common synthetic route is to use 3,5, 5-trimethylhexanoic acid, 2-bromoethanol and 4-piperidinol as raw materials, and undergo a series of esterification reactions and protective group removal reactions, the target compound TMH was generated.
Safety Information:
TMH is a relatively safe compound under general conditions. However, during the operation, care should be taken to avoid contact with skin, eyes and respiratory tract. In case of accidental contact, rinse immediately with plenty of water. In addition, TMH should be stored in a dark, dry and well-ventilated place, away from fire sources, heat sources and oxidants, and avoid mixing with other chemicals. With proper handling, TMH can be used safely.
Nature:
TMH is a colorless to pale yellow liquid with low volatility. It has low solubility, being insoluble in water, but soluble in organic solvents such as alcohols and ethers. It is a stable compound that is not easily decomposed and oxidized under regular experimental conditions.
Use:
TMH is a common organic synthesis intermediate. It is commonly used as a functional group protecting agent and reaction intermediate in organic synthesis. Its main use is in the synthesis of pharmaceutical compounds and specific chemicals such as pesticides. In addition, TMH can also be used as an additive to some polymer materials to improve the performance of the material.
Preparation Method:
The preparation methods of TMH are varied, and the most commonly used method is synthesis by chemical synthesis. A common synthetic route is to use 3,5, 5-trimethylhexanoic acid, 2-bromoethanol and 4-piperidinol as raw materials, and undergo a series of esterification reactions and protective group removal reactions, the target compound TMH was generated.
Safety Information:
TMH is a relatively safe compound under general conditions. However, during the operation, care should be taken to avoid contact with skin, eyes and respiratory tract. In case of accidental contact, rinse immediately with plenty of water. In addition, TMH should be stored in a dark, dry and well-ventilated place, away from fire sources, heat sources and oxidants, and avoid mixing with other chemicals. With proper handling, TMH can be used safely.
Last Update：2024-04-09 20:52:54
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