-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole phosphate
(S)-2,3,5,6-tetrahydro-6-phenylimidazo[2,1-b]thiazoletriylium phosphate
CAS: 32093-35-9;49548-36-9
Molecular Formula: C11H15N2O4PS
-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole phosphate - Names and Identifiers
-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole phosphate - Physico-chemical Properties
| Molecular Formula | C11H15N2O4PS |
| Molar Mass | 302.29 |
| Use | Used as anthelmintic |
-6-Phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole phosphate - Introduction
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate((S)-2,3,5, [2,1-b]thiazoletriylium phosphate), also known as imazole phosphate, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate is a white to light yellow crystalline powder or particle with the structure of imidazole ring and thiazole ring. It exhibits significant optical rotation in solution, hence the name levamisole. Its chemical formula is C17H13N4S2O4P.
Use:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate has some important applications in chemical and biological sciences. It can be used for the study and analysis of chiral properties, and also as a catalyst precursor. In addition, it can also be used in the synthesis of other chiral compounds in organic synthesis.
Method:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate can be synthesized by a variety of methods. One of the commonly used methods is to react the imidazole and thiazole derivatives with an excess of phosphorus oxychloride, followed by reaction with triethylamine to give the phosphoryl sulfoxylate phosphate. Further structural modifications can be made by reaction of sulfenylates with cation exchange resins to give (S)-, 3,5, phosphonium [2,1-b] thazoletriylium phosphates.
Safety Information:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate is generally relatively safe under normal use conditions, however, users are still required to take appropriate laboratory and personal protective measures. It may be irritating to the eyes, skin and respiratory tract, so care should be taken to avoid contact during operation. At the same time, when handling or storing (S)-2,3,5, [2,1-b] thiazoletriyum phosphate, care should be taken to avoid contact with oxidants and strong acids to avoid dangerous reactions. Read and follow the relevant safety procedures before use.
Nature:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate is a white to light yellow crystalline powder or particle with the structure of imidazole ring and thiazole ring. It exhibits significant optical rotation in solution, hence the name levamisole. Its chemical formula is C17H13N4S2O4P.
Use:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate has some important applications in chemical and biological sciences. It can be used for the study and analysis of chiral properties, and also as a catalyst precursor. In addition, it can also be used in the synthesis of other chiral compounds in organic synthesis.
Method:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate can be synthesized by a variety of methods. One of the commonly used methods is to react the imidazole and thiazole derivatives with an excess of phosphorus oxychloride, followed by reaction with triethylamine to give the phosphoryl sulfoxylate phosphate. Further structural modifications can be made by reaction of sulfenylates with cation exchange resins to give (S)-, 3,5, phosphonium [2,1-b] thazoletriylium phosphates.
Safety Information:
(S)-2,3,5, [2,1-b]thiazoletriylium phosphate is generally relatively safe under normal use conditions, however, users are still required to take appropriate laboratory and personal protective measures. It may be irritating to the eyes, skin and respiratory tract, so care should be taken to avoid contact during operation. At the same time, when handling or storing (S)-2,3,5, [2,1-b] thiazoletriyum phosphate, care should be taken to avoid contact with oxidants and strong acids to avoid dangerous reactions. Read and follow the relevant safety procedures before use.
Last Update：2024-04-10 22:29:15
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