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47481

Sigma-Aldrich

Fmoc-D-Val-OH

≥98.0% (HPLC)

Synonym(s):

N-(9-Fluorenylmethoxycarbonyl)-D-valine, Fmoc-D-valine

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About This Item

Empirical Formula (Hill Notation):
C20H21NO4
CAS Number:
84624-17-9
Molecular Weight:
339.39
Beilstein/REAXYS Number:
6489548
MDL number:
MFCD00062953
UNSPSC Code:
12352209
PubChem Substance ID:
57650976
NACRES:
NA.22

Quality Level

100

assay

≥98.0% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

143-144 °C (lit.)

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

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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Certificates of Analysis (COA)

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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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