TRIMETHYLSILYLCHLOROSULPHONATE - Names and Identifiers
TRIMETHYLSILYLCHLOROSULPHONATE - Physico-chemical Properties
Molecular Formula | C3H9ClO3SSi
|
Molar Mass | 188.71 |
Density | 1.225g/mLat 25°C(lit.) |
Melting Point | −26°C(lit.) |
Boling Point | 168-169°C(lit.) |
Flash Point | 108°F |
Vapor Presure | 2.09mmHg at 25°C |
Appearance | liquid |
Specific Gravity | 1.23 |
BRN | 1763675 |
Storage Condition | Room Temprature |
Sensitive | 8: reacts rapidly with moisture, water, protic solvents |
Refractive Index | n20/D 1.424(lit.) |
TRIMETHYLSILYLCHLOROSULPHONATE - Risk and Safety
Hazard Symbols | C - Corrosive
|
Risk Codes | R10 - Flammable
R34 - Causes burns
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
|
UN IDs | UN 2920 8/PG 2 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 10-21 |
TSCA | No |
Hazard Class | 3.2 |
Packing Group | III |
TRIMETHYLSILYLCHLOROSULPHONATE - Introduction
Trimethylsilyl chlorosulfonate(Trimethylsilyl chlorosulfonate) is an organosilicon compound with the chemical formula (CH3)3 SiSO2Cl. The following is a description of its nature, use, preparation and safety information:
Nature:
Trimethylsilyl chlorosulfonate is a colorless to pale yellow liquid with a pungent odor. It is a strong oxidant and strong acid, easy to react with water, alcohols and amines. It has a boiling point of 157-161°C and a density of about 1.21g/cm3.
Use:
Trimethylsilyl chlorosulfonate have a variety of applications in chemical synthesis. It is often used as a reagent for the introduction of sulfuric acid groups (sulfonate) to convert substituents in alcohols, phenols, amines and other compounds into sulfonic acid groups. This transformation helps to increase the activity or change the chemical properties of the compound. For example, Trimethylsilyl chlorosulfonate can silylate the enol, thereby increasing its stability; it can also convert the phenolic substituent to a sulfonic acid group, increasing the hydrophilicity of the compound. In addition, it can also be used as a catalyst in organic synthesis reactions.
Preparation Method:
Trimethylsilyl chlorosulfonate is usually obtained by reacting chlorine sulfate and trimethylchlorosilane at low temperature. Since the by-products generated by the reaction of chlorine sulfate and trimethylchlorosilane at room temperature will decompose and Trimethylsilyl chlorosulfonate, the reaction needs to be carried out at a low temperature (-70°C) to avoid side reactions.
Safety Information:
Trimethylsilyl chlorosulfonate is an irritating chemical that can cause irritation in contact with skin and eyes and can cause respiratory discomfort. Wear protective gloves, goggles and respiratory protective equipment during use. It should be stored in a cool, dry place, away from fire and oxidizing agents.
Last Update:2024-04-10 22:29:15