Fmoc-Gly-OH-2,2-D2

Product Name Fmoc-Gly-OH-2,2-D2
CAT No. CS-BX-00348
CAS No. 284665-11-8
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCC(=O)O
InchIKey NDKDFTQNXLHCGO-KNXIQCGSSA-N
Inchl InChI=1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)/i9D2
IUPAC 2,2-dideuterio-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic acid
Controlled No
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Fmoc-Gly-OH-2,2-D2 is a chemical compound that is used in peptide synthesis. It is a derivative of glycine which is an α-amino acid that is commonly found in proteins. Fmoc-Gly-OH-2,2-D2 is used as a building block in the synthesis of peptides that contain glycine residues. The chemical formula of Fmoc-Gly-OH-2,2-D2 is C18H17D2NO5. It is a deuterated derivative of Fmoc-Gly-OH which means that it contains deuterium atoms instead of hydrogen. Deuterium is an isotope of hydrogen that is twice as heavy as regular hydrogen and is often used in labeling experiments to track the movement of atoms in chemical reactions. Fmoc-Gly-OH-2,2-D2 is a solid white powder that is soluble in organic solvents such as DMF, DMSO, and CHCl3. It has a molecular weight of 339.39 g/mol and a melting point of 175-180°C. In peptide synthesis, Fmoc-Gly-OH-2,2-D2 is typically used as a protected amino acid. The Fmoc group protects the amino group of the glycine residue, allowing for selective activation of the carboxylic acid group during peptide bond formation. Overall, Fmoc-Gly-OH-2,2-D2 is a useful tool in the field of peptide synthesis and its deuterated form can be used in labeling experiments to track the movement of atoms in chemical reactions.

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