1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL&
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL&
CAS: 19753-67-4
Molecular Formula: C23H23OP
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL& - Names and Identifiers
| Name | 1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL& |
| Synonyms | 2-Butanone, 3-methyl-1-(triphenylphosphoranylidene)- |
| CAS | 19753-67-4 |
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL& - Physico-chemical Properties
| Molecular Formula | C23H23OP |
| Molar Mass | 346.4 |
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL& - Upstream Downstream Industry
| Downstream Products | GRAMISTEROL 3-METHYL-1-BUTYNE |
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL& - Introduction
1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL is an organic compound with a chemical formula of C19H16P and a molecular weight of 282.3g/mol. It is an electrophilic reagent that is commonly used in the reaction of olefins with nucleophiles in organic synthesis. It can be used as a donor of two carbon anions and react with electrophilic reagents to generate new carbon-carbon bonds.
The method for preparing 1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL can be prepared by reacting triphenylphosphine with a base without a proton, and then further reacting with a carbon-centered nucleophile. The more common method is the reaction of triphenylphosphine with an alkali carbon base to give the desired product under appropriate conditions.
Regarding safety information, 1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL is an organic compound and should follow the safety procedures for conventional organic reagents. It may be irritating to the skin, eyes and respiratory tract, so wear appropriate personal protective equipment and avoid direct contact when using it. In addition, it should also be stored in a cool, dry, well-ventilated place, away from fire and oxidizing agents. During handling and storage, care should be taken to prevent it from coming into contact with moisture in the air to avoid unnecessary chemical reactions.
The method for preparing 1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL can be prepared by reacting triphenylphosphine with a base without a proton, and then further reacting with a carbon-centered nucleophile. The more common method is the reaction of triphenylphosphine with an alkali carbon base to give the desired product under appropriate conditions.
Regarding safety information, 1-(TRIPHENYLPHOSPHORANYLIDENE)-3-METHYL is an organic compound and should follow the safety procedures for conventional organic reagents. It may be irritating to the skin, eyes and respiratory tract, so wear appropriate personal protective equipment and avoid direct contact when using it. In addition, it should also be stored in a cool, dry, well-ventilated place, away from fire and oxidizing agents. During handling and storage, care should be taken to prevent it from coming into contact with moisture in the air to avoid unnecessary chemical reactions.
Last Update：2024-04-10 22:29:15
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