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
Linear Formula: C16H17F6NO4
Product Type: Chemical
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 |
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 |