670340
Fmoc-五氟-L-苯丙氨酸
≥97%
别名:
(S)-2-(Fmoc-氨基)-3-(五氟苯基)丙酸
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关于此项目
经验公式（希尔记法）:
C24H16F5NO4
化学文摘社编号:
分子量:
477.38
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
InChI
1S/C24H16F5NO4/c25-18-15(19(26)21(28)22(29)20(18)27)9-17(23(31)32)30-24(33)34-10-16-13-7-3-1-5-11(13)12-6-2-4-8-14(12)16/h1-8,16-17H,9-10H2,(H,30,33)(H,31,32)/t17-/m0/s1
SMILES string
OC(=O)[C@H](Cc1c(F)c(F)c(F)c(F)c1F)NC(=O)OCC2c3ccccc3-c4ccccc24
InChI key
DLOGILOIJKBYKA-KRWDZBQOSA-N
assay
≥97%
optical activity
[α]/D -20.5±1.0°, c = 1 in methanol
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Quality Level
hcodes
Hazard Classifications
Aquatic Chronic 4
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Lee Schnaider et al.
ACS applied materials & interfaces, 11(24), 21334-21342 (2019-05-29)
The rapid advancement of peptide- and amino-acid-based nanotechnology offers new approaches for the development of biomedical materials. The utilization of fluorenylmethyloxycarbonyl (Fmoc)-decorated self-assembling building blocks for antibacterial and anti-inflammatory purposes represents promising advancements in this field. Here, we present the
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