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Available Variants1 g
CHA.38839-1g
Price
€242.40
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.38839-1g | €242.40 |
97%, solid
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) | C20H30ClP |
|---|---|
| CAS Number | 157282-19-4 |
| Molecular Weight | 336.88 |
| UNSPSC Code | 12352101 |
| PubChem Substance ID | 329765183 |
| NACRES | NA.22 |
| MDL number | MFCD18910707 |
Safety Information Handling visibility
| pictograms |
GHS02
GHS08
GHS05
GHS07
    GHS02,GHS08,GHS05,GHS07
|
|---|---|
| signalword | Danger |
| hcodes | H261,H314,H317,H351,H372,H373,H420 |
| pcodes | P231 + P232 - P260 - P280 - P303 + P361 + P353 - P305 + P351 + P338 - P502 |
| target_organs | Liver,Kidney |
| supp_hazards | EUH014 |
| Storage Class | 4.3 - Hazardous materials which set free flammable gases upon contact with water |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| Hazard Classifications | Carc. 2 - Eye Dam. 1 - Ozone 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 1 - STOT RE 2 Inhalation - Water-react. 3 |
Technical Overview & Applications Use-case context
Di(1-adamantyl)chlorophosphine, with the CAS registry number 157282-19-4, is a phosphorus-based organometallic compound that has garnered significant attention in the realm of organophosphorus chemistry. This compound is characterized by the presence of two bulky 1-adamantyl groups attached to a central phosphorus atom, which is also bonded to a chlorine atom. The unique steric properties imparted by the adamantyl groups confer distinct reactivity patterns to this compound, making it a valuable precursor for the synthesis of various phosphorus-containing molecules. Di(1-adamantyl)chlorophosphine has been employed in the preparation of phosphine ligands, which are crucial components in homogeneous catalysis, and its reactivity has been explored in various phosphorus-centered reactions, highlighting its potential as a versatile building block in organophosphorus chemistry. Its properties and applications continue to be the subject of ongoing research and development.
