所有图片(1)
别名:
N-(9-芴甲氧羰基)-D-缬氨酸, Fmoc-D-缬氨酸
经验公式（希尔记法）:
C20H21NO4
CAS号:
分子量:
339.39
Beilstein:
6489548
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
检测方案
≥98.0% (HPLC)
反应适用性
reaction type: Fmoc solid-phase peptide synthesis
mp
143-144 °C (lit.)
应用
peptide synthesis
官能团
Fmoc
储存温度
2-8°C
SMILES字符串
CC(C)[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI
1S/C20H21NO4/c1-12(2)18(19(22)23)21-20(24)25-11-17-15-9-5-3-7-13(15)14-8-4-6-10-16(14)17/h3-10,12,17-18H,11H2,1-2H3,(H,21,24)(H,22,23)/t18-/m1/s1
InChI key
UGNIYGNGCNXHTR-GOSISDBHSA-N
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相关类别
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WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts
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