Ordering
Available Variants25 g
CHA.61301-25g
Price
€155.20
Available – Dispatch in 14 days
100 g
CHA.61301-100g
Price
€584.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.61301-25g | €155.20 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 g | CHA.61301-100g | €584.80 |
99%
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 | CH3COCH=P(C6H5)3 |
|---|---|
| CAS Number | 1439-36-7 |
| Molecular Weight | 318.35 |
| UNSPSC Code | 12352115 |
| NACRES | NA.22 |
| PubChem Substance ID | 24849772 |
| EC Number | 215-878-2 |
| Beilstein/REAXYS Number | 750077 |
| MDL number | MFCD00008774 |
| Assay | 99% |
| Form | solid |
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
1-(Triphenylphosphoranylidene)-2-propanone, also known as CAS 1439-36-7, is a chemical compound that has been utilized in various organic synthesis reactions. This reagent is a phosphorane, a class of compounds that are known for their ability to facilitate the formation of carbon-carbon bonds. The compounds structure consists of a phosphorus atom bonded to three phenyl groups and a ketone moiety, which enables it to act as a nucleophile and participate in reactions such as the Wittig reaction. As a result, 1-(Triphenylphosphoranylidene)-2-propanone has been employed in the synthesis of a range of organic molecules, including alkenes, alkynes, and other functionalized compounds. Its versatility and reactivity make it a valuable tool in the field of organic chemistry, allowing researchers to access complex molecular structures through efficient and selective reactions.
