Chloroformic acid methyl ester

Chemical Designations - Synonyms Chlorocarbonic acid, methyl ester Chloroformic acid, methyl ester Methyl chlorocarbonate Chemical Formula CICOOCH3... [Pg.256]

S-Methyl thiourea Chloroformic acid methyl ester 3,4-Diamino-diphenyl-thioether... [Pg.621]

Methyl-isoxazole-(3)-carboxylic acid chloride 4-(/3-Aminoethyl)benzene sulfonamide hydrochloride Chloroformic acid methyl ester N-Amlno-hexamethylene imine... [Pg.732]

There is obtained from 4-[)3-[5-methyl-isoxazolyl-(3)-carboxamido]-ethyl]-benzene-sulfonamide (prepared from 5-methyl-isoxazole-(3)-carboxylic acid chloride and 4-()3-aminoethyl)-benzene-sulfonamide hydrochloride, MP 213° to 214°C in pyridine) and chloroformic acid methyl ester, in a yield of 69%, the compound N-[ [-4-[)3-[5-methyl-isoxazolyl-(3)-carbox-amido] -ethyl] ] -benzene-sulfonyl] ] -methyl-urethane in the form of colorless crystals of MP 173°C. [Pg.732]

Chloroformic acid methyl ester Fenbendazole Glisoxepid... [Pg.1623]

Chloroformic Acid, Methyl Ester Methyl Chloroformate... [Pg.34]

The Weinreb amide syntheses in Figure 6.50 proceeding via the stable tetrahedral intermediates B and F are chemoselective SN reactions at the carboxyl carbon atom of carbon acid derivatives that are based on strategy 1 of the chemistry of carboxylic acid derivatives outlined in Figure 6.41. Strategy 2 of the chemistry of carboxylic acid derivatives in Figure 6.41 also has a counterpart in carbon acid derivatives, as is demonstrated by a chemoselective acylation of an organolithium compound with chloroformic acid methyl ester in this chapter s final example ... [Pg.318]

SYNS CHLORAMEISENSAEURE METHYLESTER (GERMAN) CHLOROCARBONATE de METHYLE (FRENCH) CHLOROCARBONIC ACID METHYL ESTER CHLOROFORMIC ACID METHYL ESTER MCF METHOXYCARBONYL CHLORIDE METHYLCHLOORFORMIAT pUTCH) METHYL CHLOROFORMATE pOT) METILCLOROFORMIATO (ITALIAN) RCRA WASTE NUMBER LT56... [Pg.911]

CHLOROFORMIC ACID METHYL ESTER see MIGOOO CHLOROFORMIC ACID 1-NAPHTHYL ESTER see... [Pg.1577]

It is prepared by the reaction of sodium or potassium thiocyanate with chloroformic acid methyl ester, and the intermediate product reacts with o-phenylene diamine to form the thiophanate. Thiophanate-methyl is a colourless, crystalline compound hardly soluble in water. It forms unstable salts and complexes with bivalent ions in alkaline solutions. The range of action of each thioallophanic acid derivative is identical with that of the benzimidazole derivative into which it is converted in the plant. Thiophanate-methyl has both a preventive and a curative action. [Pg.396]

CHLOROFORMIC ACID, METHYL ESTER (79-22-1) CjHjClOj Highly flammable liquid. Forms explosive mixture with air [explosion limits in air (vol %) 6.7 to uel unknown flash point 54°F/12°C autoignition temp 842°F/450°C Fire Rating 3]. Reacts with moisture in air, forming HCl fumes. Reacts with water or steam, releasing hydrochloric acid, carbon dioxide gas, and... [Pg.244]

Polyvinylidene Fluorides (PVDF) Chloroformic Acid Methyl Ester ... [Pg.1606]

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