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AA16486

116611-64-4 | Fmoc-His-OH

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $12.00 $8.00 -   +
5g 97% in stock $33.00 $23.00 -   +
10g 97% in stock $46.00 $32.00 -   +
25g 97% in stock $96.00 $67.00 -   +
500g 97% in stock $1,909.00 $1,336.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA16486
Chemical Name: Fmoc-His-OH
CAS Number: 116611-64-4
Molecular Formula: C21H19N3O4
Molecular Weight: 377.3933
MDL Number: MFCD00190885
SMILES: O=C(N[C@H](C(=O)O)Cc1c[nH]cn1)OCC1c2ccccc2-c2c1cccc2

 

Upstream Synthesis Route
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid, commonly referred to as $name$, serves as a key building block in chemical synthesis processes. Its unique structure and properties make it a valuable tool in organic chemistry for the creation of complex molecules and compounds. In particular, $name$ is frequently used as a chiral starting material in the asymmetric synthesis of pharmaceuticals, agrochemicals, and materials with specific stereochemical requirements. By incorporating (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1H-imidazol-4-yl)propanoic acid into synthesis pathways, chemists can access enantiomerically pure compounds and control the spatial arrangement of atoms with precision. This enables the production of high-purity substances with tailored properties and has significant implications for drug discovery, materials science, and other fields that rely on molecular design.
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