Ordering
Available Variants100 mg
CHA.54386-100mg
Price
€104.80
Available – Dispatch in 14 days
500 mg
CHA.54386-500mg
Price
€440.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
100 mg | CHA.54386-100mg | €104.80 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.54386-500mg | €440.80 |
derivatization grade (chiral), LiChropur™, ≥99.0%
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 | C6H5C(OCH3)(CF3)COCl |
|---|---|
| CAS Number | 39637-99-5 |
| Molecular Weight | 252.62 |
| UNSPSC Code | 23151817 |
| NACRES | NA.22 |
| PubChem Substance ID | 329760054 |
| MDL number | MFCD00044400 |
| Beilstein/REAXYS Number | 3591563 |
| Assay | ≥99.0% (AT), ≥99.0% |
Safety Information Handling visibility
| pictograms |
GHS05
 GHS05
|
|---|---|
| signalword | Danger |
| hcodes | H314 |
| pcodes | P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405 |
| Hazard Classifications | Skin Corr. 1B |
| Storage Class | 8A - Combustible corrosive hazardous materials |
| wgk | WGK 3 |
| flash_point_f | 192.2 °F - closed cup |
| flash_point_c | 89 °C - closed cup |
| ppe | Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter |
Technical Overview & Applications Use-case context
(R)-(−)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride, with the CAS number 39637-99-5, is a chemical compound that has garnered significant attention in various scientific fields. This compound is a chiral molecule, exhibiting optical activity due to the presence of a stereocenter. Its molecular structure consists of a phenylacetyl chloride backbone, substituted with a methoxy group and a trifluoromethyl group, which impart unique chemical and physical properties. The compound is commonly utilized as a reagent in organic synthesis, particularly in the preparation of chiral molecules and pharmaceuticals. Its reactivity and selectivity make it a valuable tool for chemists, allowing for the creation of complex molecules with high enantiopurity. The compounds properties and applications are extensively studied and documented in scientific literature, highlighting its importance in modern chemistry.
