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Available Variants1 g
CHA.57904-1g
Price
€75.52
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.57904-1g | €75.52 |
98%
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) | C12H15F3O2 |
|---|---|
| CAS Number | 51800-98-7 |
| Molecular Weight | 248.24 |
| UNSPSC Code | 12352115 |
| NACRES | NA.22 |
| PubChem Substance ID | 24851361 |
| EC Number | 257-429-3 |
| Beilstein/REAXYS Number | 6779716 |
| MDL number | MFCD00003746 |
| Assay | 98% |
| Form | liquid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319,H335 |
| pcodes | P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 10 - Combustible liquids |
| wgk | WGK 3 |
| flash_point_f | 179.6 °F - closed cup |
| flash_point_c | 82 °C - closed cup |
| ppe | Eyeshields, Gloves, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(+)-3-(Trifluoroacetyl)camphor, with the CAS number 51800-98-7, is a synthetic organic compound that has been utilized as a chiral auxiliary in various asymmetric synthesis reactions. This compound is derived from camphor, a naturally occurring bicyclic ketone, and has been modified with a trifluoroacetyl group at the 3-position. The incorporation of the trifluoroacetyl moiety imparts unique properties to the molecule, including increased reactivity and selectivity in certain chemical transformations. As a result, (+)-3-(Trifluoroacetyl)camphor has been employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where high levels of stereochemical control are required. Its utility in asymmetric synthesis has made it a valuable reagent in the field of organic chemistry, particularly in the context of enantioselective reactions.
