Ethyl hydrosulfide

Athyl-jodid, n, ethyl iodide, iodoethane. -rho-danid, n, ethyl thiocyanate, -rot, n. ethyl red. -schwefelsaure, /, ethylsulfurie acid, -senfol, n, ethyl mustard oil (CsHcNCS). -sulfhydrat, n, ethyl hydrosulfide, -verbindung, /, ethyl compound, -wasserstoff,... [Pg.37]

Synonyms AI3-26618 BME EINECS 200-837-3 Ethanethiol Ethyl hydrosulfide Ethyl hydrosulphide Ethyl sulfhydrate Ethyl thioalcohol FCY LPG ethyl mercap-tan 1010 Mercaptoethane 1-Mercaptoethane NSC 93877 0-2712 NSC 29026 SCC Thio-ethanol Thioethyl alcohol UN 2363... [Pg.584]

Synonyms Ethanethiol ethyl hydrosulfide ethyl sulfhydrate ethyl thioalcohol thio-ethanol thioethyl alcohol... [Pg.336]

S-ETHYL-HOMOCYSTEINE see EEIOOO S-ETHYL-dl-HOMOCYSTEINE see EEIOOO ETHYL HYDKATE see EFUOOO ETHYL HYDRIDE see EDZOOO ETHYL HYDROGEN PEROXIDE see ELDOOO ETHYL HYDROPEROXIDE see ELDOOO ETHYL HYDROPERSULFIDE see EEBOOO ETHYL HYDROSULFIDE see EMBIOO ETHYL HYDROXIDE see EFUOOO ETHYL-p-HYDROXYBENZOATE see HJLOOO 2-ETHYL-3-(p-HYDROXYBENZOYL)BENZOFUKAN see BBJ500... [Pg.1682]

ETHYL HYDROSULFIDE (75-08-1) Forms explosive mixture with air (flash point <0°F/<— 18°C). Reacts with water, steam acids, acid fumes, forming hydrogen sulfide. Violent reaction with strong oxidizers, calcium hypochlorite. Incompatible with aliphatic amines, caustics, ethylene oxide, isocyanates, nitric acid, sulfuric acid. Attacks some forms of plastics, coatings, and rubber. Flow or agitation of substance may generate electrostatic charges due to low conductivity. [Pg.537]

Aethanethiol Aethylmercaptan AI3-26618 EINECS 200-837-3 Etantiolo Ethaanthiol Ethanethiol Ethyl hydrosulfide Ethyl mercaptan Ethyl suifhydrate Ethyl thioalcohol Ethylmercaptaan Ethyimerkaptan Etilmerc-aptano HSDB 814 LPG ethyl mercaptan 1010 Mercaptoethane 1-Mercaptoethane NSC 93877 Thio-ethanol Thioethyl alcohol UN236S Used to impart odor to natural gas, in manufacture of pesticides, plastics and antioxidants. Volatile liquid mp = -147,8° bpn 36,1° d = 0,8315 slightly soluble in H2O, more soluble in organic solvents, Alofina S/gma-Aldrich Fine Chem. US. BioChem. [Pg.276]

Ethyl hydrosulfide. See Ethyl mercaptan Ethyl hydroxide. See Alcohol Ethyl 2-hydroxybenzoate. See Ethyl salicylate Ethyl 4-hydroxybenzoate. See Ethylparaben Ethyl-o-hydroxybenzoate. See Ethyl salicylate Ethyl p-hydroxybenzoate. See Ethylparaben Ethyl-4-hydroxybenzoate potassium salt. See Potassium ethylparaben Ethyl 3-hydroxybutanoate. See Ethyl 3-hydroxybutyrate Ethyl 3-hydroxybutyrate CAS 5405-41-4 EINECS/ELINCS 226-456-2 FEMA 3428... [Pg.1750]

Phenylacetamide has been obtained by a wide variety of reactions from benzyl cyanide with water at 250-260° 6 from benzyl cyanide with water and cadmium oxide at 240° 6 from benzyl cyanide with sulfuric acid 7 8 by saturation of an acetone solution of benzyl cyanide with potassium hydrosulfide 9 from benzyl cyanide with sodium peroxide 10 by electrolytic reduction of benzyl cyanide in sodium hydroxide 11 from ethyl phenyl-acetate with alcoholic 12 or aqueous 13 ammonia from phenyl-acetic acid with ammonium acetate 14 or urea 15 from diazoacetophenone with ammoniacal silver solution 16 from phenyl-acetic acid imino ether hydrochloride and water 17 from acetophenone with ammonium poly sulfide at 215° 18 from benzoic acid 19 and by heating the ammonium salt of phenyl-acetic acid.20... [Pg.94]

Ethyl mercaptan is raw stock for the synthesis of 2-oxydiethylsulfide. It is formed by the interaction of ethylchloride with sodium hydrosulfide according to the reaction ... [Pg.448]

The reaction of ethyl (5)-(4-chloro-3-pyridyl)xanthate (544) with sodium hydrosulfide gave l,3-dithiolo[4,5-c]pyridine-2-thione (545) along with 3,4-dithiolpyridine (546) (Equation (50))... [Pg.336]

Hydrosulfide end groups are usually introduced with potassium ethyl xanthogenate in acetone, thus substituting a bromide atom by a dithio carbonic acid. The latter is reductively cleaved by sodium borohydride in the presence of amines (Scheme 2.6). [Pg.11]

Potassium ethyl xanthate, 837 Potassium ferricyanide, 409,9J9-933,1239 Potassium fluoride, 375, 933-935 Potassium hydride in oil, 935 Potassium hydrosulfide, 935 Potassium hydroxide, 935-937 Potassium hydroxide-Acetone, 938 Potassium hypochlorite, 488, 938 Potassium manganate, 938-939 Potassium 2-methyl-2-butoxide, 574, 905, 939-940... [Pg.725]

Chloropyridopyrimidines readily undergo amination reactions with ammonia,9-11,13> 86>41, 48,50,78, 110,122,128,126,127aliphaticamines,9-11, i3,48,so,no,i2d, 127 and aromatic amines9, 11,48,50,110,122 to yield mono- or diaminopyridopyrimidines or 4-amino-2-ehloro derivatives. Selective replacement of chloro substituents, however, was not achieved with the reaction of dimethylamine and 2,4-dichloropyrido-[2,3-d]pyrimidine.110 Thionation reactions by means of thiourea,10, 36, no, 122 hydrosulfide ion, 9 13,48,°0,56 sodium ethyl sulfide,10 replacement by alkoxide,10,13,36,38,60 and hydrolysis9,10,13,60 to regenerate the pyridopyrimidone all take place readily. Reductive dehalogenation10 to yield pyrido[3,2-d]pyrimidine (2) has been claimed but disputed.33... [Pg.95]

The prior to imiversal synthesis to this kind of product was reported in 1910 by Senary [27] as the multi step reaction of ethyl 4-chloro-2-( ano-3-oxobutanoate (1). After the treatment of 1 with potassium hydrosulfide the reactive sufanyl-substituted intermediate 2 was created, which in the subsequent intramolecular addition of sulfanyl group to cyano group proceeded ethyl 2-amino-4-hydroxythiophene-3-carboxylate (4) in equilibrium with its cyclic tautomer - the appropriate imine 3 (Scheme 1). [Pg.5]

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