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2-methoxypropyl

Chemical Name 1 -[3-(Chloromercuri)-2-methoxypropyl] urea Common Name Chlormeroprin... [Pg.309]

Chemical Name [3-[[ [(3-carboxy-1-oxopropyl)amino] carbonyl] amino] -2-methoxypropyl] -hydroxymercury mixture with 3,7-dihydro-1,3-dimethyl-1 H-purine-2,6-dione... [Pg.947]

Mercury(II) acetate in acetic acid reacts with allyl chloride and methanol to produce 3-chloro-2-methoxypropyl mercuric acetate, C1CH2CH(0CH3)-CH2Hg0C(=0)CH3. The compound is difficult to isolate from the solution and generally an ammoniacal solution is used for commercial applications. [Pg.563]

H-1-BENZOPYRAN-3-CARBOXYLIC ACID, 8-(3 (HYDROXYMERCURI)-2-METHOXYPROPYL)-2-0X0-. SODIUM SALT, compd. with THEOPHYLLINE (1 1)... [Pg.227]

Common Name [3-[3-(3-Carboxypropionyl)ureido]-2-methoxypropyl] hydroxymercury mixture with theophylline... [Pg.2181]

Hydroxymethylation of ketone (155) was followed by protection of the aliphatic hydroxy group (2-methoxypropyl ether) and addition of an a-benzyloxymethylene group at C-4. Acidic workup at the last stage of the reaction sequence produced (156). Its transformation to aldehyde (157) was carried out by successive treatment with methoxypropyl ether, acetic anhydride and pyridine, hydrochloric acid and methanol, and finally chromic acid, pyridine and hydrochloric acid. Dehydration of (157) led to the formation of (158) in 20% yield. Reagents other than the mentioned produced appreciable quantities of the cis A/B isomer. The butenolide (159) was finally synthesized by oxidation and hydrogenolysis. In order to complete the synthesis of triptolide it was necessary to introduce the... [Pg.203]

Lovenberg, Buchanan, and Rabinowitz (65) tested the response of ferredoxin to mercury compounds. Two mercurial reagents used, p-mer-curibenzoate (PCMB) and o-((3-hydroxymercuri-2-methoxypropyl)car-bamyl)phenoxyacetate (sodium mersalyl) reacted rapidly with ferredoxin and caused a bleaching of the visible spectrum and a concomitant loss of biological activity. C. pasteurianum ferredoxin was titrated with PCMB as described by Boyer (24) and the results showed that 20 moles of PCMB reacted with 1 mole of ferredoxin. In another determination, 2 moles of PCMB reacted with 1 mole of sodium sulfide. Since ferredoxin contained 7 moles of inorganic sulfide and 8 moles of half-cystine residues, 22 (7 x 2 = 14 14 + 8 = 22) moles of PCMB would be expected to react with 1 mole of ferredoxin. These data, summarized in Table 8, are consistent with the existence of two types of sulfur in ferredoxin. This conclusion was supported by the presence of half-cystine residues in ferredoxin after inorganic sulfide had been removed by acid hydrolysis, as well as results of sulfur analyses, which showed an amount of sulfur greater than could be attributed to half-cystine residues. [Pg.125]

Condensation of cyclopentanone with the amino ester (205) gives 1,3-dimethyl-1,2,3,5,6,7-hexahydro-4/7-l-pyrindin-4-one (206), in 38% yield, which can be reduced to the octahydro derivative with lithium aluminum hydride.139 A variety of substituted 4-pyrindones (203, 204, 207-209) is obtained by heating 2-methoxypropyl 1-cyclopenten-l-yl... [Pg.226]

P-METHOXY)PROPYLCAMPHORAMIC ACID DISODIUM SALT DISODIUM-N-(3-(CARBOXYMETHYLTHIO-MERCURI)-2-METHOXYPROPYL)-a-CAMPHORAMATE... [Pg.1336]

HYDROXYMERCURI-2-METHOXYPROPYL)CARB.- MOYL)PHENOXYACETI C ACID MONOSODIUM SAI.T see SIH500 N-(y-HYDROXYMERCURI-P-... [Pg.1725]

SODIUM o-((3-(HYDROXYMERCURI)-2-METHOXYPROPYL)CARBAMOYL)PHENOXY ACETATE see SIH500 SODIUM HYPOCHLORITE see SHU500 SODIUM HYPOPHOSPHITE see SHVOOO SODIUM HYPOSULFITE see SKIOOO SODIUM INOSINATE see DXE500 SODIUM-5 -INOSINATE see DXE500 SODIUM IODIDE see SHWOOO SODIUM IODINE see SHWOOO SODIUM ISOAMYLETHYL BARBITURATE see AON750... [Pg.1883]

Magnesium ions are essential for superprecipitation. This is borne out by the fact that an excess of EDTA (ethylenediaminetetraacetic acid) leads to complete inhibition. Another powerful inhibitor of superprecipitation is the sodium salt of o-[(3-hydroxymercuri-2-methoxypropyl)car-bamoyl]phenoxyacetic acid ( Salyrgan ). [Pg.14]

The Polish proprietary medicine Dehydrit is described in Gehe s Codex (3rd supplement, 1950) as the sodium salt of o-[(3-hydroxymercuri-2-methoxypropyl) carbamyl]phenoxyacetic acid dissolved in aqueous itheophylline solution. This preparation is known in the U. S. Pharmacopeia as Mersalyl and theophylline injection, and in the U. S. Dispensatory (page 700, 24th edition) the pharmacist is informed of the United States equivalent in the form of Salyrgan-Theophylline Ampuls (Winthrop). [Pg.123]

Butanoic acid, 4-((( 2-methoxypropyl)amino)carbonyl)-amino)-4-OXO-, mercury complex Dilurgen N-((3-(Hydroxymercuri)-2-methoxypropyl)carbamoyl)-succlnamic acid and theophylline Meralluride Meralluridum Meralurida Mercardan Mercuhydrin Mercurate(l-), (3-((((3-carboxylato-1-oxopropyl)amino)-... [Pg.386]

Occasionally it is more profitable to treat the methoxy-bromomercuri or methoxyiodomercuri compound with iodine, which can be done in boiling methanol, aqueous methanol, or carbon tetrachloride, e.g., in the conversion of A-allylphthalimide into the A-(3-halo-2-methoxypropyl)-phthalimide. [Pg.140]

Early version of the ketal resist system (KRS) from IBM partially 2-methoxypropyl (ketal)-protected PHOST, partially 2-benzyloxypropyl (ketal)-protected PHOST. [Pg.382]

Chloro (2-methoxy-3-uriedopropyl) mercury" Hg Mercury Hg, [3-(aminocarbonyl) amino] 2-methoxypropyl] chloro-USP BPC (1959) ... [Pg.439]

See other pages where 2-methoxypropyl is mentioned: [Pg.623]    [Pg.432]    [Pg.623]    [Pg.476]    [Pg.800]    [Pg.633]    [Pg.672]    [Pg.967]    [Pg.800]    [Pg.4256]    [Pg.1260]    [Pg.1564]    [Pg.1656]    [Pg.58]    [Pg.922]    [Pg.922]    [Pg.923]    [Pg.927]    [Pg.246]    [Pg.386]    [Pg.140]    [Pg.789]    [Pg.4255]    [Pg.2398]   


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