Composés polycycliques

Please enquire for more information about 7-Chloro-2-(2,4-dimethylphenyl)-8-methylquinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 5-Fluoroindole-3-butyric Acid is used in preparation of Aminochroman and Aminotetralin derivatives, which are useful in the treatment of serotonin-mediated disorders. References Hatzenbuhler, N., et al.: PCT Int. Appl., (2005);

Please enquire for more information about 6-Benzyloxy-1H-indazole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about tert-Butyl 6-bromo-1-oxo-3,4-dihydroisoquinoline-2(1H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Lactone

Please enquire for more information about 5,5'-Bis(trifluoromethyl)-2,2'-bipyridyl including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-Chloro-7-methyl-3-(5-methyl-1,2,4-oxadiazol-3-yl)quinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

(±)-Decursinol (3',4'-dihydro-3'-hydroxy-Xanthyletin) is a natural product from Angelica gigas.

Please enquire for more information about 1-Acetyl-6-nitro-1,2,3,4-tetrahydroquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

In this experimental study, 7-Bromo-5-methylindoline-2,3-dione has been shown to interact with a square of rotations. It was found that 7-Bromo-5-methylindoline-2,3-dione interacts with the square in a monolithic way. The experimental study showed that the molecule is not affected by the rotation and is unaffected by the shape of the square.

Please enquire for more information about Methyl 7-cyclopropyl-1-ethyl-2-mercapto-4-oxo-1,4-dihydropyrido[2,3-d]pyrimidine-5-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-Bromoquinoline-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about tert-Butyl 6-(hydroxymethyl)-1H-indole-1-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-Formylindoline is an organic compound that reacts with formamide in the presence of a strong acid to produce N-formylglycine. It can be used as a formylating agent, which is a chemical compound that contains the formyl group (HC=O). This reaction occurs at room temperature and does not require an acid catalyst, unlike other reactions that form amides. Formylation is a reaction in which the formyl group replaces one or more hydrogen atoms on carbon atoms of an organic molecule. N-Formylindoline has been shown to react with tripeptides and carbon tetrachloride to produce endoplasmic reticulum peptides. The reaction system for this process includes mammalian cells and plates (96 well) for assays.

Please enquire for more information about 3-(Pyrido[2,3-e]pyrrolo[1,2-a]pyrazin-6-ylthio)propanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 3-Amino-3-benzyl-3,4-dihydroquinolin-2(1H)-one

Please enquire for more information about Ethyl-4-fluoroindole-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Lactone

Please enquire for more information about 5-Methoxy-1H-indazole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Chloropyrido[3,4-d]pyrimidine is a heterocyclic compound that belongs to the pyrimidine family. It can be synthesized by reacting 2-chloro-3-nitropyridine with potassium tert-butoxide in an aqueous solution of ethanol. 4-Chloropyrido[3,4-d]pyrimidine can be converted into other heterocycles by different methods and has been used as a synthon for many other pyrimidines. This functional group has five members, which are interconnected by single bonds and form a ring system with alternating single and double bonds. The 5 atoms of this ring system are arranged in the shape of a pyramid (trigonal). There are two isomers: 4-(2,6) and 4-(2,5).

2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester is a synthetic compound that can be used as a reagent in the synthesis of polynucleotides and polypeptides. It can also be used as an inhibitor of ketoreductase, which is an enzyme involved in the synthesis of fatty acids and ketones. 2-[3-(S)-[3-(2-(7-Chloro-2-quinolinyl)ethenyl)phenyl]-3-hydroxypropyl]benzoic acid methyl ester has been shown to inhibit the growth of wild type and mutant strains of E. coli. The molecular weight of this compound is 439.

Please enquire for more information about 1-Benzyl-3-hydroxy-1H-indazole sodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Isoquinoline-7-carboxylicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Borabicyclo[3.3.1]nonane is a functional group that has been used in the synthesis of α-pinene and other terpenoids. Borabicyclo[3.3.1]nonane can be synthesized by reacting α-pinene with methoxy groups and amines at high temperatures in the presence of a catalyst, such as boron trifluoride etherate. The reaction mechanism involves an elimination reaction followed by an addition reaction to form a lactam ring, which is then hydrolyzed to release 9-borabicyclo[3.3.1]nonane. This functional group has been used for the synthesis of α-pinene, which is a monoterpene found in pine needles and oil from turpentine trees, among other sources. The structural analysis shows that these molecules are linear chains with reactive sp2 hybridized carbons and hydroxyl groups on one end and alk

Please enquire for more information about 4-Chloro-2,6-bis(trifluoromethyl)quinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

Applications 6-Chloro-4-(2-cyclopropylethynyl)-3,4-dihydro-3-(phenylsulfonyl)-4-(trifluoromethyl)-2(1H)-quinolinone is an intermediate in the synthesis of novel quinolinones as HIV-1 reverse transcriptase inhibitors. References Patel, M., et al.: Bioorg. Med. Chem. Lett., 11, 1943 (2001);

Please enquire for more information about 5-Methoxy-1,2,3,4-tetrahydroquinoline hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2-(3-Morpholin-4-ylpropyl)-1-oxo-1,2,3,4,5,6-hexahydro-3a,5-epoxyisoindole-7-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-(Methylsulfonyl)indoline-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page