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Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L -alanine
产品别名
2120095-23-8
Boc-3-[3,4-bis(trifluoromethyl)phenyl]-
(S)-3-(3,4-Bis(trifluoromethyl)phenyl)-2-(tert-butoxycarbonylamino)propanoic acid
结构式
基本信息
| Empirical Formula【经验(实验)分子式】 | C16H17F6NO4 |
| Molecular weight | 401.30 |
| PubChem Substance ID【PubChem化学物质编号】 | 329772653 |
| NACRES | NA.22 |
| Application【应用】 | 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【其他说明】 | Ligand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids |
产品性质
| Quality Level【质量水平】 | 100 |
| description【描述】 | ALPH: +24.0, 0.5%EtOH |
| Assay【测定】 | ≥95% (HPLC) |
| form【形式】 | powder or solid |
| reaction suitability | reaction type: Boc solid-phase peptide synthesis reagent type: ligand reaction type: C-H Activation |
| application(s) | peptide synthesis |
| storage temp.【储存温度】 | 2-8℃ |
| SMILES string | OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC(C(F)(F)F)=C(C(F)(F)F)C=C1)=O |
| InChI | 1S/C16H17F6NO4/c1-14(2,3)27-13(26)23-11(12(24)25)7-8-4-5-9(15(17,18)19)10(6-8)16(20,21)22/h4-6,11H,7H2,1-3H3,(H,23,26)(H,24,25)/t11-/m0/s1 |
| InChI key | LLRXWQAYIGATCH-NSHDSACASA-N |
| packaging【包装】 | 1 g in glass bottle |
安全信息
| Pictograms【象形图】 | GHS07 |
| Signal word【警示用语：】 | Warning |
| Hazard Statements | H315 - H319 - H335 |
| Precautionary Statements | P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications【危险分类】 | Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| Target Organs【靶器官】 | Respiratory system |
| Storage Class Code【储存分类代码】 | 11 - Combustible Solids |
| WGK | WGK 3 |
