ALD00348
Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L -alanine
≥95% (HPLC)
别名:
(S)-3-(3,4-Bis(trifluoromethyl)phenyl)-2-(tert-butoxycarbonylamino)propanoic acid
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关于此项目
经验公式（希尔记法）:
C16H17F6NO4
化学文摘社编号:
分子量:
401.30
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
eCl@ss:
32150313
description
ALPH: +24.0, 0.5%EtOH
Quality Segment
assay
≥95% (HPLC)
form
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.
2-8°C
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
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).
警示词
Warning
危险代码
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
存储类别
11 - Combustible Solids
WGK
WGK 3
闪点 (F)
Not applicable
闪点 (°C)
Not applicable