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Available Variants1 g
CHA.28541-1g
Price
€93.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
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Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.28541-1g | €93.60 |
Professionally catalogued chemical listing prepared to support identification, technical review, safety visibility, and structured B2B sourcing workflows.
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
| Empirical Formula (Hill Notation) | C20H15OP |
|---|---|
| CAS Number | 15596-07-3 |
| Molecular Weight | 302.31 |
| NACRES | NA.22 |
| PubChem Substance ID | 329760846 |
| UNSPSC Code | 12352002 |
| MDL number | MFCD00040613 |
| Form | solid |
Safety Information Handling visibility
| Storage Class | 11 - Combustible Solids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
(Triphenylphosphoranylidene)ketene, also known as CAS 15596-07-3, is a chemical compound that has garnered significant attention in the realm of organic synthesis. This ketene is a highly reactive intermediate that can participate in various cycloaddition reactions, making it a valuable tool for constructing complex molecular frameworks. The compounds unique electronic properties, which arise from the presence of the triphenylphosphoranylidene moiety, enable it to engage in efficient and selective reactions with a range of substrates. As a result, (triphenylphosphoranylidene)ketene has found applications in the synthesis of heterocyclic compounds, natural products, and other complex molecules, highlighting its potential as a versatile building block in modern organic chemistry. Its reactivity and selectivity make it an attractive reagent for chemists seeking to develop innovative synthetic methodologies.
