(BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE
Benzoylmethylenetriphenylphosphorane
CAS: 859-65-4
Molecular Formula: C26H21OP
(BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE - Names and Identifiers
| Name | Benzoylmethylenetriphenylphosphorane |
| Synonyms | skf45359 phenacylidenetriphenylphosphorane Benzoylmethylenetriphenylphosphorane (BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE (Benzoylmethylene)triphenylphosphorane 2-(triphenylphosphoranylidene)-acetophenon 2-(TRIPHENYLPHOSPHORANYLIDENE)ACETOPHENONE alpha-(Triphenylphosphoranylidene)acetophenone 1-phenyl-2-(triphenylphosphoranylidene)ethanone 1-phenyl-2-(triphenylphosphoranylidene)-ethanon 1-phenyl-2-(triphenyl-lambda~5~-phosphanylidene)ethanone |
| CAS | 859-65-4 |
| EINECS | 212-727-2 |
| InChI | InChI=1/C26H21OP/c27-26(22-13-5-1-6-14-22)21-28(23-15-7-2-8-16-23,24-17-9-3-10-18-24)25-19-11-4-12-20-25/h1-21H |
(BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE - Physico-chemical Properties
| Molecular Formula | C26H21OP |
| Molar Mass | 380.42 |
| Density | 1.18±0.1 g/cm3(Predicted) |
| Melting Point | 183-186°C |
| Boling Point | 550.9±33.0 °C(Predicted) |
| Flash Point | 287°C |
| Solubility | Soluble in Methanol (almost transparency). |
| Vapor Presure | 3.48E-12mmHg at 25°C |
| Appearance | Crystalline |
| Color | White to Light yellow |
| BRN | 620285 |
| Storage Condition | Inert atmosphere,2-8°C |
| Sensitive | Air Sensitive |
| Refractive Index | 1.646 |
| MDL | MFCD00014088 |
(BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE - Risk and Safety
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37 - Wear suitable gloves. |
| RTECS | AN0540000 |
| HS Code | 29319000 |
(BENZOYLMETHYLENE)TRIPHENYLPHOSPHORANE - Introduction
Benzoylmethylenetriphenylphosphorane(Benzoylmethylenetriphenylphosphorane) is an organic compound whose molecular formula is C27H21OP. The following is a description of its nature, use, preparation and safety information:
Nature:
Benzoylmethylenetriphenylphosphorane is a colorless to light yellow crystal. It can be dissolved in organic solvents such as ethanol and dimethylformamide at room temperature, but it is insoluble in water. It is a compound with unique electronic properties in a spatial configuration.
Use:
Benzoylmethylenetriphenylphosphorane is often used as a reaction reagent in organic synthesis, including Horner-Wadsworth-Emmons reaction and Wittig reaction. It can react with aldehydes or ketones to form olefinic compounds containing double bonds. In addition, it can also be used in the synthesis of drugs, biologically active compounds and other key steps in organic synthesis.
Preparation Method:
The preparation method of Benzoylmethylenetriphenylphosphorane is usually obtained by reacting benzoylformic acid thioester with triphenylphosphine bromide. The reaction is generally carried out in an anhydrous organic solvent such as dimethylformamide or tetrahydrofuran. After completion of the reaction, the product can be purified by crystallization or column chromatography.
Safety Information:
Benzoylmethylenetriphenylphosphorane are generally relatively safe under normal conditions of use. However, as an organic compound, it still has a certain potential danger. Care should be taken to follow basic laboratory safety practices, such as wearing appropriate protective equipment (such as gloves and glasses) to prevent contact with skin and eyes. In addition, in contact with other chemicals, especially strong oxidants and combustibles, special care should be taken to prevent unexpected reactions and accidents. Handle and store in a well-ventilated place and avoid prolonged contact with air, water and moisture.
Nature:
Benzoylmethylenetriphenylphosphorane is a colorless to light yellow crystal. It can be dissolved in organic solvents such as ethanol and dimethylformamide at room temperature, but it is insoluble in water. It is a compound with unique electronic properties in a spatial configuration.
Use:
Benzoylmethylenetriphenylphosphorane is often used as a reaction reagent in organic synthesis, including Horner-Wadsworth-Emmons reaction and Wittig reaction. It can react with aldehydes or ketones to form olefinic compounds containing double bonds. In addition, it can also be used in the synthesis of drugs, biologically active compounds and other key steps in organic synthesis.
Preparation Method:
The preparation method of Benzoylmethylenetriphenylphosphorane is usually obtained by reacting benzoylformic acid thioester with triphenylphosphine bromide. The reaction is generally carried out in an anhydrous organic solvent such as dimethylformamide or tetrahydrofuran. After completion of the reaction, the product can be purified by crystallization or column chromatography.
Safety Information:
Benzoylmethylenetriphenylphosphorane are generally relatively safe under normal conditions of use. However, as an organic compound, it still has a certain potential danger. Care should be taken to follow basic laboratory safety practices, such as wearing appropriate protective equipment (such as gloves and glasses) to prevent contact with skin and eyes. In addition, in contact with other chemicals, especially strong oxidants and combustibles, special care should be taken to prevent unexpected reactions and accidents. Handle and store in a well-ventilated place and avoid prolonged contact with air, water and moisture.
Last Update：2024-04-09 20:52:54
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Product Name: (Benzoylmethylene)Triphenylphosphorane Visit Supplier Webpage Request for quotationCAS: 859-65-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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