47691
Fmoc-α-Me-Ala-OH
≥97.0% (HPLC)
Synonym(s):
Fmoc-α-aminoisobutyric acid, Fmoc-α-methylalanine
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C19H19NO4
CAS Number:
Molecular Weight:
325.36
Beilstein:
5604328
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service