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Merck
CN

772062

Sigma-Aldrich

Fmoc-D-Met-OH

98%

Synonym(s):

Fmoc-D-methionine

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About This Item

Empirical Formula (Hill Notation):
C20H21NO4S
CAS Number:
112883-40-6
Molecular Weight:
371.45
Beilstein:
5384578
MDL number:
MFCD00062958
UNSPSC Code:
12352200
PubChem Substance ID:
329767536
NACRES:
NA.26

Key Documents

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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

SMILES string

CSCC[C@@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

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

InChI key

BUBGAUHBELNDEW-GOSISDBHSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKBN7925V

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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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