Ordering
Available Variants5 g
CHA.47244-5g
Price
€71.92
Available – Dispatch in 14 days
25 g
CHA.47244-25g
Price
€162.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.47244-5g | €71.92 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.47244-25g | €162.40 |
97%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | (C6H5)3P=CHCO2CH2C6H5 |
|---|---|
| CAS Number | 15097-38-8 |
| Molecular Weight | 410.44 |
| NACRES | NA.22 |
| PubChem Substance ID | 24866098 |
| UNSPSC Code | 12352108 |
| MDL number | MFCD00191787 |
| Assay | 97% |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves, type N95 (US) |
Technical Overview & Applications Use-case context
Benzyl(triphenylphosphoranylidene)acetate, with the CAS registry number 15097-38-8, is a chemical compound that has garnered significant attention in the realm of organic synthesis. This reagent is commonly utilized in various reactions, including the synthesis of complex molecules and the formation of carbon-carbon bonds. The compounds unique structure, featuring a phosphoranylidene moiety, enables it to participate in a range of chemical transformations, making it a valuable tool for chemists. Its applications are diverse, spanning multiple fields of chemistry, and its properties have been extensively studied and documented in the scientific literature. As a result, benzyl(triphenylphosphoranylidene)acetate has become a staple in many laboratories, facilitating the development of new synthetic methodologies and the advancement of chemical research. Its versatility and efficacy have solidified its position as a key reagent in modern organic synthesis.
