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Benzylidyne chloride

Synonyms Benzenyl chloride benzoic trichloride benzylidyne chloride benzyl trichloride phenylchloroform toluene trichloride trichlorotoluene (trichloromethyl)-... [Pg.78]

Synonyms. Benzenyl chloride benzenyl trichloride benzylidyne chloride benzyl trichloride phenyl chloroform phenyltrichloromethane toluene trichloride trichloro-methylbenzene... [Pg.457]

SYNS BENZENYL CHLORIDE BENZENYL TRICHLORIDE BENZOIC TRICHLORIDE BENZOTRICHLORIDE pOT, MAK) BENZYLIDYNE CHLORIDE CHLORURE de BENZENYLE (FRENCH) PHENYL CHLOROFORM PHENYLTRICHLORO-METHANE RCRA WASTE NUMBER U023 ... [Pg.157]

BENZYLIDYNE CHLORIDE (98-07-7) Combustible liquid (flash point 260°F/127°C). Reacts with moist air, forming hydrogen chloride fumes. Reacts slowly with water, forming corrosive hydrochloric acid and benzoic acid. Reacts violently with amines or finely divided light metals (aluminum, magnesium, beryllium, etc.). Contact with acids evolves chlorine gas. Attacks some plastics, rubber, and coatings. Attacks metals in the presence of moisture. [Pg.174]

Beilstein Handbook Reference) AI3-02583 Benzene, trichloromethyl)- Benzenyl trichloride Benzoic trichloride Benzotrichloride Benzolrlcloruro Benzyl trichloride Benzylidyne chloride BRN 0508152 CCRIS 1292 Chloruie de benzenyle Chlorure de benzylidyne EINECS 202-634-5 HSDB 2076 NSC 14663 Phenyl chloroform Phenyltrichloromethane RCRA waste a,a,a,-trichloro- Toluene trichloride ... [Pg.62]

Synonyms Benzene, (trichloromethyl)- Benzenyl chloride Benzenyl trichloride Benzoic trichloride Benzylidyne chloride Benzyl trichloride Phenylchloroform Phenyl trichloromethane Toluene trichloride Toluene,... [Pg.458]

Benzylidyne chloride. See Benzotrichloride Benzylidyne fluoride. See Benzotrifluoride Benzyl isoamyl alcohol. See a-Isobutylphenethyl alcohol Benzyl isoamyl ether CAS 122-73-6 EINECS/ELINCS 204-570-3 Synonyms Benzene, [(3-methylbutoxy) methyl]- Benzyl isopentyl ether Ether, benzyl isopentyl Isoamyl benzyl ether Isopentyl benzyl ether Empirical C12H18O... [Pg.474]

The nitration of sensitive compounds with dinitrogen pentoxide has the advantage of avoiding the use of strong acids or aqueous conditions this has been exploited in the nitration of benzylidyne trichloride and benzoyl chloride, which reacted in carbon tetrachloride smoothly and without hydrolysis. [Pg.52]

See other pages where Benzylidyne chloride is mentioned: [Pg.131]    [Pg.131]    [Pg.240]    [Pg.234]    [Pg.58]   
See also in sourсe #XX -- [ Pg.78 ]



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