Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L-alanine
ALDRICH/ALD00348 - ≥95% (HPLC)
Synonym: (S)
CAS Number: 2120095-23-8
Empirical Formula (Hill Notation): C16H17F6NO4
Molecular Weight: 401.30
MDL Number: MFCD29049357
Linear Formula: C16H17F6NO4
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: ALD00348-1G
| application(s) | peptide synthesis |
| assay | ≥95% (HPLC) |
| description | ALPH: +24.0, 0.5%EtOH |
| form | powder or solid |
| InChI | 1S/C16H17F6NO4/c1-14(2,3) |
| InChI key | LLRXWQAYIGATCH-NSHDSACASA |
| Quality Level | 100  |
| reaction suitability | reaction type: Boc solid-phase peptide synthesis |
| reagent type: ligand reaction type: C-H Activation |
|
| SMILES string | OC([C@@H](NC(OC(C)(C)C)=O |
| storage temp. | 2-8°C |
| Application: | Unnatural amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835). |
| Other Notes: | Ligand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids  |
| Packaging: | 1 g in glass bottle |
| Symbol |  GHS07 |
| Signal word | Warning |
| Hazard statements | H315 - H319 - H335 |
| Precautionary statements | P302 + P352 - P305 + P351 + P338 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | ≥95% (HPLC) |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352209 |