Building Blocks

<p>Stability Moisture Sensitive<br>Applications A phosphorylating agent.<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 Sartori: Chem. Rev., 48, (1951), Nachmansohn, et al.: Adv. Enzymology, 12, 259 (1951)<br></p>

<p>Applications Intermediate in the preparation of Alfentanil.<br>References Kudzma, L., et al.: J. Med. Chem., 32, 2534 (1989),<br></p>

<p>Stability Moisture sensitive<br>Applications Diisopropyl Phosphorochloridate is a phosphorylating agent.<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 Sartori: Chem. Rev., 48, (1951), Nachmansohn, et al.: Adv. Enzymology, 12, 259 (1951)<br></p>

<p>Applications 4-(1H-1,2,4-triazol-1-yl)phenol (cas# 68337-15-5) is a useful research chemical.<br></p>

<p>Applications An analogue of Carbamazepine (C175840). The toxicity of Cyheptamide in mice and rats is very low, and anticonvulsant activity is marked. Carbamazepine and Cyheptamide have certain stereochemical features in common with Phenytoin.<br>References Platt, D.S., et al.: Biochem. Pharmacol., 18, 429 (1969), Kraml, M., et al.: Biochem. Pharmacology, 20, 2327 (1971),<br></p>

<p>Applications 2,2’-Thiodiethanol is a reagent used in the synthesis of water soluble gold-N-heterocyclic carbene complexes for catalytic homogenous acid.<br>References Ibrahim, H. et al.: Adv. Synth. Catal., 357 ,3893 (2015);<br></p>

<p>Applications A Sulfamethoxazole metabolite.<br>References Gill, H., et al.: Br. J. Clin. Pharmacol., 42, 347 (1996), Winter, H., et al.: Clin. Pharmacol. Ther., 76, 579 (2004), Vyas, P., et al.: Biochem. Pharmacol., 70, 275 (2005), Vyas, P., et al.: Drug Metab. Dispos., 34, 16 (2006),<br></p>

<p>Applications 1,4-Cyclohexanedimethanol is extensively used as cross-linking reagent in polymer industry. It has been used in the synthesis of polyketal copolymers. It was used as diol comonomer during the synthesis of polyester-carbonates based on 1,3-propylene-co-1,4-cyclohexanedimethylene succinate.<br>References Yang, S., et al.: Bioconjugate Chem., 19, 1164 (2008); Liu, Y., et al.: J. Polym. Sci. A Polym. Chem., 39, 2508 (2011); Hungria, A., et al.: Angewandte Chemie, 45, 4782 (2006)<br></p>

<p>Applications 1-(2-Pyridyl)piperazine is a compound that belongs to a class of selective α2-adrenoceptor antagonists. 1-(2-Pyridyl)piperazine shows sympatholytic activity. 1-(2-Pyridyl)piperazine is also a metabolite of Azaperone (A802200).<br>References Saari, W.S. et al.: J. Med. Chem., 26, 1696 (1983); Caccia, S. et al.: J. Chrom., 283, 211 (1984);<br></p>

<p>Applications N-(2,6-Diisopropylphenylcarbamoylmethyl)iminodiacetic Acid (cas# 65717-97-7) is a compound useful in organic synthesis.<br></p>

<p>Applications 6,7-Dihydro-6-mercapto-5H-pyrazolo[1,2-a][1,2,4]-triazolium chloride (cas# 153851-71-9) is a useful research chemical.<br></p>

<p>Applications 4-Sulfamoylbenzoic Acid is used as a reagent in the synthesis of carbonic anhydrase inhibitors anticonvulsant agents.<br>References Singh, S. et al.: J. Enz. Inhib. Med. Chem., 31, 417 (2016);<br></p>

<p>Stability Hygroscopic<br>Applications Nitrosophenidylate is an N-nitroso derivative of Methylphenidate Hydrochloride(M325880), which is a controlled substance (stimulant). CNS stimulant. Four isomers of Methylphenidate are known to exist. One pair of threo isomers and one pair of erythro are distinguished, from which only d-threo-Methylphenidate exhibits the pharmacologically usually desired effects. This compound is a 4:1 mixture of rac-erythro (M325670) and rac-threo (M325671).<br>References Greenblatt, E.N., et al.: J. Pharmacol. Exp. Ther., 131, 115 (1961), Padmanabhan, G.R., Anal. Profiles Drug Subs., 10, 473 (1981), Srinivas, N.R., et al.: Pharm. Res., 10, 14 (1993),<br></p>

<p>Applications 10-NONADECANONE (cas# 504-57-4) is a useful research chemical.<br></p>

<p>Applications N,N-Diethylbutyramide is a compound that has been used as a pretreatment before N,N-Dimethyltryptamine (D469620) to decrease its hallucinogenic activity.<br>References Smythies, J.R., et al.: Eur. J. Pharmacol., 17, 270-2 (1972);<br></p>