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3- Chloroallyl chloride

Synonyms BRN 1719558 /7 a/ 5-3-Chloroallyl chloride ( )-l,3-Dichloropropene lra/ 5-l,3-Di-chloropropene ( )-l,3-Dichloro-l-propene rra/ 5-l,3-Dichloro-l-propene 1,3-Dichlororoprop-l-ene /ra/ 5-l,3-Dichloro-l-propylene NSC 6202 EPA pesticide chemical code 029001 RCRA waste number U084 ra/ s-Telone Telone 2000 Telone C Telone C 17 Telone 11 UN 2047. [Pg.437]

Chloroacetophenone, see a-Chloroacetophenone Q-Chloroacetophenone, see a-Chloroacetophenone cfs-3-Chloroallyl chloride, see cfs-l,2-Dichloropropylene frarrs-3-Chloroallyl chloride, see frarrs-l,2-Dichloro-... [Pg.1471]

DOWICIL 100 QUATERNIUM 15 3,5,7-TRIAZA-l-AZONIAADAMANTANE, l-(3-CHLOROALLYL)-, CHLORIDE... [Pg.319]

CHLOROALLYL CHLORIDE (542-75-6) Forms explosive mixture with air (flash point 9.5°F/35°C). Reacts violently with strong oxidizers. Incompatible with strong acids, oxidizers, active metals, aluminum or magnesium compounds, aliphatic amines, alkanolamines, alkaline materials. Flow or agitation of substance may generate electrostatic charges due to low conductivity. [Pg.286]

SYNONYMS 3-chloroallyl chloride, alpha-chloroallyl chloride, 3-chloropropenyl chloride, DCP, telone, vidden-D. [Pg.75]

SYNONYMS 1,3-dichloropropene, 3-chloroallyl chloride, 3-chloropropenyl chloride, telone, vidden, alpha-chloroallyl chloride, gamma-chloroallyl chloride, NCI-C03985, vidden d, DCP, d-D92, l,3-dichloro-2-propene, dorlone 11... [Pg.301]

Synonyms/Trade Names 3-Chloroallyl chloride DCP 1,3-Dichloro-1-propene 1,3-Dichloropropylene Telone ... [Pg.101]

Negishi first observed the insertion of the y-halolithium species 75 obtained by deprotonation of propargyl chloride into octylzirconocene chloride protonation of the product afforded the allene 79 (Scheme 3.20) [37]. The overall effect is insertion of an allenyl carbenoid. The a-halolithium equivalent 76 is conveniently generated by addition of two equivalents of base to 2-chloroallyl chloride [52] and affords the same products. The organome-tallic product 77 of allenyl carbenoid insertion is either in equilibrium with the propargyl... [Pg.94]

Synonyms 1,3-DCP a-chloroallyl chloride 1,3-dichloropropylene Telone Telone II DD fumigants... [Pg.235]

SYNS a-CHLOROALLYL CHLORIDE y-CHLOROALLYL CHLORIDE DICHLOROPROPENE pOT) 1,3-DICHLOROPROPy ENE-l DICHLOROPROPYLENE a,7-DICHLOROPROPYLENE 1,3-DICHLOROPROPYLENE NCI-C03985 RCRA WASTE NUMBER U084 TELONE TELONE II SOIL FUMIGANT VIDDEN D... [Pg.470]

Synonyms a-Chloroallyl chloride y-Chloroallyl chloride 1,3-Dichloropropene Dichloropropylene 1,3-Dichloropropylene a,Y-Dichloropropylene... [Pg.1275]

With mercuric salt catalysts, hydrogen chloride adds to give 2-chloroallyl alcohol, 2-chloroprop-2-en-l-ol [5976-47-6] (27). [Pg.104]

Formaldthyde Arylsulfonamide resin, chloroallyl-hexaminium chloride... [Pg.309]

Cationic surfactants contain a positively charged headgroup and are typically used as conditioners to improve hair manageability and reduce static. Cationic surfactants are especially irritating to eyes when used in high concentrations but are safe and useful in low amounts. Quatemium-15 (chloroallyl methanamine chloride, Fig. 7.9.4) is a cationic surfactant included in shampoo formulations... [Pg.98]

Figure 7.9.4 The cationic surfactant quatemium-15 (chloroallyl methanamine chloride). Figure 7.9.4 The cationic surfactant quatemium-15 (chloroallyl methanamine chloride).
Synthesis. Oxidation of -alkyl or -benzyl IJ,IJ-dialkylthio-carbamates with one equivalent of m-chloroperoxybenzoic acid (MCPBA) in chloroform or methylene chloride at -25° to 25°C yields the corresponding carbamoyl sulfoxide (3) in essentially quantitative yield (3-5). The -chloroallyl thiocarbamate sulfoxides (e.g., 4-7) are obtained in the same manner except that the temperature is maintained between -20°C and 0°C for the oxidation and extraction of the reaction mixture with 5% sodium carbonate aqueous solution (7, 8). [Pg.66]

Chloroallyl) thiocarbamate sulfoxides (. ., 5-2) un-.doubtedly rearrange in an analogous manner but in tbis case tbe sulfenate quickly undergoes an additional 1,2-elimination reaction (7 ). Tbe resulting products are tbe IJ, -dialkylcarbamoyl-sulfenyl chloride (M) and tbe carbonyl compound, aldehydes... [Pg.69]

Synthesis. Oxidation of -chloroallyl dlthlocarbamates with equimolar MCPBA In chloroform, methylene chloride or methanol at -25°C gives a very exothermic reaction leading to the corresponding dithlocarbamate sulflnes (15) . sulfallate sulflne ( )... [Pg.71]

Miscellaneous compounds l-(3-Chloroallyl)-3,5,7-triaza-l-azoniaadamantane chloride 2,3,5,6-Tetrachloro-4-(methyl-sulfonyl)pyridine... [Pg.399]

Chloroallyl)-3,5,7-triaza-l-azoniaadamantane chloride Copper 8-hydroxyquinolinate... [Pg.411]

Furans can be prepared by acid catalyzed cyclization of masked 1,4-diketones. /3-Chloroallyl ketones which are obtained by alkylation of enamines or enolate ions behave as masked 1,4-diketones and afford furans on treatment with acid (67JA4557). 2,4-Dialkyl-furans (40) have been prepared by cyclization of the 3-chloroallyl ketone (39), which may be obtained by acylation of allyl chlorides (73KGS1434). [Pg.661]


See other pages where 3- Chloroallyl chloride is mentioned: [Pg.434]    [Pg.1916]    [Pg.296]    [Pg.1013]    [Pg.434]    [Pg.1573]    [Pg.1916]    [Pg.235]    [Pg.235]    [Pg.236]    [Pg.236]    [Pg.286]    [Pg.286]    [Pg.484]    [Pg.131]    [Pg.296]    [Pg.1013]    [Pg.878]    [Pg.197]    [Pg.134]    [Pg.897]    [Pg.118]    [Pg.69]    [Pg.80]    [Pg.81]    [Pg.186]    [Pg.897]    [Pg.101]   
See also in sourсe #XX -- [ Pg.101 ]




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Chloroallylation

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