Boc-3-[3,4-bis(trifluoromethyl)phenyl]-<sc>L</sc>-alanine

产品名称：

2120095-23-8
Boc-3-[3,4-bis(trifluoromethyl)phenyl]-L-alanine
(S)-3-(3,4-Bis(trifluoromethyl)phenyl)-2-(tert-butoxycarbonylamino)propanoic acid

产品介绍：

产品说明

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).

包装

1 g in glass bottle

其他说明

Ligand-Controlled C(sp³)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids

基本信息

经验(实验)分子式	C₁₆H₁₇F₆NO₄
分子量	401.30
PubChem化学物质编号	329772653
NACRES	NA.22

产品性质

质量水平	100
描述	ALPH: +24.0, 0.5%EtOH
测定	≥95% (HPLC)
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
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

安全信息

象形图
警示用语：	Warning
危险声明	H315 - H319 - H335
预防措施声明	P302 + P352 - P305 + P351 + P338
危险分类	Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官	Respiratory system
储存分类代码	11 - Combustible Solids
WGK	WGK 3
闪点(F)	Not applicable
闪点(C)	Not applicable