Ethyl-1-Methyl-5-sulfaMoyl-1H- pyrazole-4-carboxyalte - Names and Identifiers
Ethyl-1-Methyl-5-sulfaMoyl-1H- pyrazole-4-carboxyalte - Physico-chemical Properties
Molecular Formula | C6H9N3O4S
|
Molar Mass | 219.22 |
Density | 1.62 |
Boling Point | 447.7±55.0 °C(Predicted) |
pKa | 9.49±0.60(Predicted) |
Storage Condition | Room Temprature |
Physical and Chemical Properties | Acidity coefficient (pKa) 9.49±0.60(Predicted) |
Ethyl-1-Methyl-5-sulfaMoyl-1H- pyrazole-4-carboxyalte - Introduction
It is an organic compound with the formula C9H11N3O4S. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: White or off-white crystalline powder.
-Melting point: about 184-187 degrees Celsius.
-Solubility: Good solubility in common organic solvents.
Use:
-is an important intermediate compound, which can be used to synthesize biologically active compounds.
-In the field of medicine, it is used as a starting material for drug synthesis and also as an intermediate for drugs.
-In addition, it can also be used for conversion reactions in organic synthesis.
Preparation Method:
The synthesis of
-or can be achieved by a variety of methods, depending on the starting materials and conditions required.
-A common synthesis method is to react 1-methyl-4-ethoxypyrazole with an electrophile, such as formic anhydride, and then introduce a sulfonamide group under acidic conditions.
Safety Information:
-Toxicological and safety data are limited, so it is necessary to follow general laboratory safety practices when using or handling this compound.
-Wear appropriate personal protective equipment such as lab coats, gloves, and glasses when performing synthesis or manipulation.
-This compound may cause irritation and sensitivity to human health. Avoid inhalation, ingestion or contact with skin and eyes.
-In the event of unexpected exposure or discomfort, seek medical help immediately and provide your doctor with detailed information about the compound.
Last Update:2024-04-09 20:52:54