Composti policiclici

<p>Applications 3-(2-Deoxy-5-O-phosphono-β-D-erythro-pentofuranosyl)-3,4-dihydro-5H-imidazo[2,1-i]purine-5-thione is used in the synthesis of azidoetheno analogs of deoxyadenosine as nucleotide photo-affinity probes.<br>References Flaherty, D. et al.: Nucleos. Nucleot., 14, 65 (1995);<br></p>

<p>Stability Hygrscopic<br>Applications 2,2'-Biquinoline-4,4-dicarboxylic acid disodium salt<br></p>

<p>Applications Methyl quinoline-4-carboxylate (cas# 21233-61-4) is a useful research chemical.<br></p>

<p>Applications Ethyl 4,6,8-trichloroquinoline-3-carboxylate<br></p>

<p>Applications 6-Fluoroquinoline, is a versatile building block used in the synthesis of various chemical compounds.<br></p>

<p>Applications 2,6-Dichloro-9-nitroso-9H-purine is a compound useful in organic synthesis.<br></p>

<p>Applications 4-Hydroxy-quinoline-6-carboxylic acid<br></p>

<p>Applications tert-Butyl 1,6-Diazaspiro[3.4]octane-1-carboxylate is a reactant in the preparation of N-(3-pyridinyl) spirocyclic diamines as ligands for nicotinic acetylcholine receptors.<br>References Sippy, K.B., et. al.: Bioorg. Med. Chem. Lett., 19, 1682 (2009)<br></p>

<p>Applications 3-(quinolin-2-yl)propanoic acid (cas# 39111-94-9) is a useful research chemical for biological study. In particular it has been used in identifying structure-activity relationship of HDAC6 zinc-finger ubiquitin binding domain inhibitors.<br>References Ferreira, F., et al.: J. Med. Chem, 61, 4517 (2018)<br></p>

<p>Applications 6-Hydroxyindole-2-carboxylic acid (cas# 40047-23-2) is a useful research chemical.<br></p>

<p>The bicyclo[2.2.1]hept-2-ylethanone is an isomer of the bicyclo[2.2.1]heptane, with a ketone group in place of a methylene group on one ring. It is a mixture of two isomers: the cis and trans form, which are in equilibrium with each other at room temperature. The equilibrium constants for this reaction are Kcis = 6.6×10 and Ktrans = 1.4×10 at 25°C and pH 7, respectively, which means that the trans isomer predominates at low concentrations and the cis form predominates at high concentrations.</p>