tert-Butyl (1-(phenylsulfonyl)-1H-indol-2-yl)carbamate
2-(tert-Butoxycarbonylamino)-1-(phenylsulfonyl)indole
CAS: 1020722-09-1
Molecular Formula: C19H20N2O4S
tert-Butyl (1-(phenylsulfonyl)-1H-indol-2-yl)carbamate - Names and Identifiers
tert-Butyl (1-(phenylsulfonyl)-1H-indol-2-yl)carbamate - Physico-chemical Properties
| Molecular Formula | C19H20N2O4S |
| Molar Mass | 372.44 |
| Density | 1.26±0.1 g/cm3(Predicted) |
| pKa | 12.99±0.43(Predicted) |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD09835515 |
tert-Butyl (1-(phenylsulfonyl)-1H-indol-2-yl)carbamate - Introduction
2-(tert-Butoxycarbonylamino)-1-(phenylsulfonyl)indole is an organic compound with the chemical formula C19H20N2O4S. It is a solid, soluble in some organic solvents such as chloroform and methylene chloride.
This compound is commonly used in the field of pharmaceutical research. It is a kind of amide compound with good biological activity. Some studies suggest it may have anti-inflammatory and anti-tumor activities. It also has some applications in the synthesis of organic compounds and drug design.
The method for preparing 2-(tert-Butoxycarbonylamino)-1-(phenylsulfonyl)indole is usually to react 1-benzoylindole with tert-butoxycarbonylchloramine, and then to obtain the target product by reacting sodium benzenesulfonyl sulfide with the generated product.
Regarding safety information, because there is not enough specific data to evaluate its toxicity and danger, it is necessary to take appropriate laboratory safety operations when using it. Wear protective gloves, goggles and masks during preparation and operation to ensure good ventilation and avoid inhalation, ingestion and skin contact. If touched, flush immediately with plenty of water and seek medical help.
Please note: Consult reliable chemical literature and relevant laboratory manuals for detailed information on the properties, applications and safety of this compound.
This compound is commonly used in the field of pharmaceutical research. It is a kind of amide compound with good biological activity. Some studies suggest it may have anti-inflammatory and anti-tumor activities. It also has some applications in the synthesis of organic compounds and drug design.
The method for preparing 2-(tert-Butoxycarbonylamino)-1-(phenylsulfonyl)indole is usually to react 1-benzoylindole with tert-butoxycarbonylchloramine, and then to obtain the target product by reacting sodium benzenesulfonyl sulfide with the generated product.
Regarding safety information, because there is not enough specific data to evaluate its toxicity and danger, it is necessary to take appropriate laboratory safety operations when using it. Wear protective gloves, goggles and masks during preparation and operation to ensure good ventilation and avoid inhalation, ingestion and skin contact. If touched, flush immediately with plenty of water and seek medical help.
Please note: Consult reliable chemical literature and relevant laboratory manuals for detailed information on the properties, applications and safety of this compound.
Last Update：2024-04-09 21:04:16
