CAS 104578-89-4
:2-Deoxy-N-phenyl-L-erythro-pentofuranosylamine
Description:
2-Deoxy-N-phenyl-L-erythro-pentofuranosylamine is a chemical compound characterized by its structural features, which include a furanose sugar moiety and an amine functional group. This compound is a derivative of ribose, specifically modified to include a phenyl group and a deoxy group, which indicates the absence of an oxygen atom at the 2-position of the sugar. The presence of the phenyl group contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. The L-erythro configuration suggests specific stereochemistry that can affect its biological activity and recognition by enzymes or receptors. This compound may be of interest in medicinal chemistry and biochemistry, particularly in the context of nucleoside analogs or as a potential building block for more complex molecules. Its CAS number, 104578-89-4, allows for precise identification in chemical databases and literature. Overall, the unique combination of its sugar and amine functionalities positions it as a potentially valuable compound in various chemical and pharmaceutical applications.
Formula:C11H15NO3
InChI:InChI=1/C11H15NO3/c13-7-10-9(14)6-11(15-10)12-8-4-2-1-3-5-8/h1-5,9-14H,6-7H2/t9-,10+,11?/m1/s1
InChI key:InChIKey=OYCBOKNPGJKONC-JKIOLJMWSA-N
SMILES:N(C1O[C@@H](CO)[C@H](O)C1)C2=CC=CC=C2
Synonyms:- 2-Deoxy-N-phenyl-<span class="text-smallcaps">L</span>-erythro-pentofuranosylamine
- 2-Deoxy-N-phenyl-<span class="text-smallcaps">L</span>-erythropentofuranosylamine
- 2-Deoxy-N-phenyl-L-erythropentofuranosylamine
- <span class="text-smallcaps">L</span>-erythro-Pentofuranosylamine, 2-deoxy-N-phenyl-
- L-erythro-PentofuranosylaMine, 2-deoxy-N-phenyl-
- 2-Deoxy-N-phenyl-L-erythro-pentofuranosylamine
- 2-Deoxy-L-ribose-anilide
- (2S,3R)-2-(Hydroxymethyl)-5-(phenylamino)tetrahydrofuran-3-ol
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Found 2 products.
2-Deoxy-L-ribose-anilide
CAS:<p>2-Deoxy-L-ribose-anilide is a chemical compound that has been patented for its use in the detection of magnetic fields. The patent claims that this compound can be used as an intermediate in the preparation of other compounds. 2DRA has different transition temperatures, depending on whether it is in the solid or liquid state. When 2DRA is heated, it changes from a colorless liquid to a yellow crystal at around 100°C and then becomes a white solid at around 150°C. The magnetic properties of 2DRA arise from its ability to form strong bonds with other molecules, which are broken by external magnetic fields.</p>Formula:C11H15NO3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:209.12 g/mol

