772062
Fmoc-D-Met-OH
98%
别名:
Fmoc-D-methionine
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关于此项目
经验公式（希尔记法）:
C20H21NO4S
化学文摘社编号:
分子量:
371.45
UNSPSC Code:
12352200
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5384578
InChI
1S/C20H21NO4S/c1-26-11-10-18(19(22)23)21-20(24)25-12-17-15-8-4-2-6-13(15)14-7-3-5-9-16(14)17/h2-9,17-18H,10-12H2,1H3,(H,21,24)(H,22,23)/t18-/m1/s1
SMILES string
CSCC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI key
BUBGAUHBELNDEW-GOSISDBHSA-N
assay
98%
form
powder or crystals
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
120-124 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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