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47691

Sigma-Aldrich

Fmoc-α-Me-Ala-OH

≥97.0% (HPLC)

Synonym(s):

Fmoc-α-aminoisobutyric acid, Fmoc-α-methylalanine

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About This Item

Empirical Formula (Hill Notation):
C19H19NO4
CAS Number:
94744-50-0
Molecular Weight:
325.36
Beilstein/REAXYS Number:
5604328
MDL number:
MFCD00151913
UNSPSC Code:
12352209
PubChem Substance ID:
57651082
NACRES:
NA.26

assay

≥97.0% (HPLC)

reaction suitability

reaction type: Fmoc solid-phase peptide synthesis

mp

182-188 °C

application(s)

peptide synthesis

functional group

Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C19H19NO4/c1-19(2,17(21)22)20-18(23)24-11-16-14-9-5-3-7-12(14)13-8-4-6-10-15(13)16/h3-10,16H,11H2,1-2H3,(H,20,23)(H,21,22)

InChI key

HOZZVEPRYYCBTO-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Aleksandra Balliu et al.
Chembiochem : a European journal of chemical biology, 18(14), 1396-1407 (2017-04-23)
A 42-residue polypeptide conjugated to a small-molecule organic ligand capable of targeting the phosphorylated side chain of Ser15 was shown to bind glycogen phosphorylase a (GPa) with a K

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