Halogénures organiques

<p>Stability Moisture Sensitive<br>Applications N-Phenylbis(trifluoromethanesulfonamide) is used in the enantioselective synthesis of β-amino acids via the Mannich reaction. Used in the synthesis of sphingosine 1-phosphate-1 receptor agonists useful in pharmaceutical application.<br>References Asano, M. et al.: Tetra. Asymm., 24, 449 (2013);<br></p>

<p>Applications o-phenetidine hydrochloride (cas# 89808-01-5) is a useful research chemical.<br></p>

<p>Applications 4-Bromobenzotrifluoride is an aromatic compound that is used as a reagent to synthesize Bergenin (B318650), a compound that originates in Mallotus japonicus that exhibits hepatoprotective and antioxidant effects. 4-Bromobenzotrifluoride is also used as a reagent to prepare (±)-Preclamol, a partial dopamine D2 agonist that is used to treat Parkinson’s disease.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Lim, H., et al.: Pharmacology, 63, 71 (2001); Parkan, K., et al.: Chem. Eur. J., 20, 4414 (2014); Pirtosek, Z., et al.: Clin. Neuro., 16, 550 (1993); Takahashi, H., et al.: Bioorg. Med. Chem., 11, 1781 (2003); Vasdev, N., et al.: Synapse, 60, 314 (2006)<br></p>

<p>Stability Light Sensitive<br>Applications 5-Iodo-2’-deoxytubercidin is a derivative of 7-Iodo-7-deazadenine designed to be incorporated into DNA by primers extension by using Vent(exo-) polymerase. Possesses photophysical properties.<br>References Macickova-Cahova, H., et al.: Chem. Eur. J., 17, 5833-5841 (2011); Saito, Y., et al.: Tetrahedron Lett., 52, 4726-4729 (2011)<br></p>

<p>Applications 4,6-Dibromo-2,3-dichloroaniline is a bromination product of dichloro-substituted aniline. 4,6-Dibromo-2,3-dichloroaniline is used in the preparation of benzothiazoles.<br>References Gruzdev, I.V. et al.: Rus. J. Appl. Chem., 84, 1748 (2011); Paramasivam, R.: Ind. J. Chem. Sec. B Org. Med. Incl. Med. Chem., 26B, 930 (1987);<br></p>

<p>Applications Used in asymmetric Mannich reactions by α-silyl controlled aminomethylation of ketones.<br>References Enders, D., et al.: Synlett, 644 (20000,<br></p>

<p>Applications N-​Methylcyclopropanami​ne Hydrochloride can be used as reactant/reagent in preparation of substituted benzazinones as antibacterial compounds.<br>References Jin, Q., et al.: PCT Int. Appl., WO 2017098440 A1 20170615 (2017)<br></p>

<p>Applications 5-azetidin-3-yl-3-(trifluoromethyl)-1,2,4-oxadiazole hydrochloride (cas# 1426290-78-9) is a useful research chemical.<br></p>

<p>Applications 4-Deiodo-amidotrizoic Acid can be obtained from 3,5-Dinitrobenzenemethanol. It can also be used in biological study for quality environmental risk assessment of photolytic transformation products of iodinated X-ray contrast agent diatrizoic acid.<br>References Rastogi, T., et al.: Sci. Total Environ., 482-483, 378-388 (2014);<br></p>

<p>Applications 5-Chloro-1-hexene is a reagent with difluoroacetic acid that results in the formation of 5-chloro-2-hexyl-2-d trifluoro-acetate and 1,4-chlorine shift.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Peterson, P. E., et al.: J. Am. Chem. Soc., 86, 4503-4 (1964)<br></p>

<p>Applications Bis(4-chlorobutyl) Ether is used in the alkylation of anthracene-cyanoacrylic Diels-Alder adducts.<br>References Buck, C.J. et al.: J. Polym. Sci. Polym. Chem. Ed., 16, 2475 (1978);<br></p>

<p>Applications 3,4-Dimethylbenzotrifluoride could be a useful reagent for the preparation of bromodomain targeting degronimers for target protein degradation.<br>References Phillips, A. J., et al.: PCT Int. Appl. (2017) WO 2017197056 A1<br></p>

<p>Applications 1-Chloro-4-(2,2,2-trichloroethyl)benzene is used as a compound to study effects such as singlet vs triplet reactivity of photogenerated α,n-didehydrotoluenes and as well, the polar effect in reactions with substituted benzyl radicals with carbon tetrachloride.<br>References Pedroli, C., et al.: J. Org. Chem., 82, 6592-6603 (2017); Dneprovskii, A.S., et al.: Russ. J. Organ. Chem., 35, 1495-98 (1999);<br></p>