3-(2-methylpropyl)-2-sulfanylidene-1H-quinazolin-4-one
3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone
CAS: 117038-39-8
Molecular Formula: C12H14N2OS
3-(2-methylpropyl)-2-sulfanylidene-1H-quinazolin-4-one - Names and Identifiers
3-(2-methylpropyl)-2-sulfanylidene-1H-quinazolin-4-one - Physico-chemical Properties
| Molecular Formula | C12H14N2OS |
| Molar Mass | 234.32 |
| Melting Point | 211.5～213.5℃ |
| Storage Condition | Room Temprature |
| Sensitive | IRRITANT |
| MDL | MFCD00175721 |
3-(2-methylpropyl)-2-sulfanylidene-1H-quinazolin-4-one - Introduction
3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone is an organic compound with the formula C14H16N2OS. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone as a white crystalline solid.
-Solubility: It is slightly soluble in water and soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone is a heterocyclic compound containing thiazole ring and quinazoline ring, which has a variety of biological activities. It has potential anti-tumor, anti-inflammatory and antibacterial activities in the field of medicine. It is also used as an important intermediate in organic synthesis.
Preparation Method:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone can be synthesized by various routes. A common method is the reaction of 2-aminobenzoyl propionic acid quaternary ammonium hydrofluoride with sulfonyl chloride to obtain the product after removal of the quaternary ammonium salt under alkaline conditions.
Safety Information:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone specific safety information may vary depending on the conditions and use, so the relevant safety information and applicable regulations should be consulted before use.
-Avoid inhaling its dust or vapor, and avoid contact with skin and eyes. Appropriate protective gloves and goggles should be worn when operating it.
-During storage and handling, comply with relevant chemical safety regulations and keep them away from combustibles and oxidants.
-If the compound is ingested or inhaled by mistake, seek medical attention immediately and provide the information required by the doctor.
Nature:
-Appearance: 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone as a white crystalline solid.
-Solubility: It is slightly soluble in water and soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone is a heterocyclic compound containing thiazole ring and quinazoline ring, which has a variety of biological activities. It has potential anti-tumor, anti-inflammatory and antibacterial activities in the field of medicine. It is also used as an important intermediate in organic synthesis.
Preparation Method:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone can be synthesized by various routes. A common method is the reaction of 2-aminobenzoyl propionic acid quaternary ammonium hydrofluoride with sulfonyl chloride to obtain the product after removal of the quaternary ammonium salt under alkaline conditions.
Safety Information:
- 3-Isobutyl-2-thioxo-2,3-dihydro-4(1H)-quinazolinone specific safety information may vary depending on the conditions and use, so the relevant safety information and applicable regulations should be consulted before use.
-Avoid inhaling its dust or vapor, and avoid contact with skin and eyes. Appropriate protective gloves and goggles should be worn when operating it.
-During storage and handling, comply with relevant chemical safety regulations and keep them away from combustibles and oxidants.
-If the compound is ingested or inhaled by mistake, seek medical attention immediately and provide the information required by the doctor.
Last Update：2024-04-09 19:06:00
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3-(2-methylpropyl)-2-sulfanylidene-1H-quinazolin-4-one
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Phenol, 5-amino-2,4-bis(1,1-dimethylethyl)-
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dimethyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
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30356-58-2
Phenol, 5-amino-2,4-bis(1,1-dimethylethyl)-
5-{[(3,5-dichloro-2-hydroxyphenyl)methyl]amino}-2,3-dihydro-1H-1,3-benzodiazol-2-one