4-Methyl-piperidine-1-sulfonyl chloride
4-Methyl-piperidine-1-sulfonyl chloride
CAS: 41483-70-9
Molecular Formula: C6H12ClNO2S
4-Methyl-piperidine-1-sulfonyl chloride - Names and Identifiers
| Name | 4-Methyl-piperidine-1-sulfonyl chloride |
| Synonyms | 4-methyl-1-piperidinesulfonyl chloride 4-Methyl-piperidine-1-sulfonyl chloride 1-Piperidinesulfonyl chloride, 4-methyl- |
| CAS | 41483-70-9 |
4-Methyl-piperidine-1-sulfonyl chloride - Physico-chemical Properties
| Molecular Formula | C6H12ClNO2S |
| Molar Mass | 197.68 |
| Density | 1.33±0.1 g/cm3(Predicted) |
| Boling Point | 279.2±7.0 °C(Predicted) |
| pKa | -8.21±0.40(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Sensitive | Irritant |
| MDL | MFCD08445024 |
4-Methyl-piperidine-1-sulfonyl chloride - Introduction
chloride is an organic compound with the chemical formula C6H12ClNO2S. It is a colorless or yellowish liquid compound with a pungent odor. The compounds are soluble in polar organic solvents, such as alcohols and ethers, but insoluble in water.
Salt chloride is commonly used as a reagent in organic synthesis. It can be used to synthesize compounds with pharmaceutical activity, such as amino acid derivatives and peptide compounds. In addition, it can also be used as a deprotection reagent for protecting functional groups of biological reagents.
The preparation of calcium chloride typically employs the reaction of calcium chloride hydrochloride with thionyl chloride (SOCl2) in a reaction solvent such as dimethylformamide (DMF) or dimethylsulfoxide (DMSO).
When using the chloride, pay attention to its irritation and toxicity. It can cause irritation and damage to the skin, eyes and respiratory tract. Therefore, protective equipment such as gloves, goggles and respirators should be worn during operation. In addition, the compound is flammable and requires proper storage and handling. Please observe the relevant safety procedures.
Salt chloride is commonly used as a reagent in organic synthesis. It can be used to synthesize compounds with pharmaceutical activity, such as amino acid derivatives and peptide compounds. In addition, it can also be used as a deprotection reagent for protecting functional groups of biological reagents.
The preparation of calcium chloride typically employs the reaction of calcium chloride hydrochloride with thionyl chloride (SOCl2) in a reaction solvent such as dimethylformamide (DMF) or dimethylsulfoxide (DMSO).
When using the chloride, pay attention to its irritation and toxicity. It can cause irritation and damage to the skin, eyes and respiratory tract. Therefore, protective equipment such as gloves, goggles and respirators should be worn during operation. In addition, the compound is flammable and requires proper storage and handling. Please observe the relevant safety procedures.
Last Update：2024-04-09 20:52:54
