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1- Chloro-2,3-epoxypropane,

Chloro,2,3,-Epoxypropane, see Epichlorohydrin 2- Chloroethanol, see Ethyiene chlorohydrin Chloroethylene, see Vinyl chloride Chloroform (trichloromethane) 13.0... [Pg.230]

Chloro-2,3-epoxypropane, see Epichlorohydrin Chloroethane, see Ethyl chloride Chloroethanol, see Ethylene chlorohydrin Chloromethane, see Methyl chloride Chloronaphthalene 1.19 5.6 132 >558... [Pg.120]

Chloro-2,3-epoxy propane See 1-Chloro-2,3-epoxypropane Isopropylamine... [Pg.462]

Synonyms or Alternate Names are found at die bottom of each spread in their alphabetical listing die number following die name refers to the numerical place of this compound in the table. For example, epichlorohydrin, clOl, indicates that this compound is found listed under the name 1 -chloro-2,3-epoxypropane. [Pg.80]

A mixture of the alcohol with formic acid rapidly self-heated, then reacted violently [1], A stirred mixture with cyanoacetic acid exploded violently after application of heat [2]. Contact with acids causes self-condensation of the alcohol, which may be explosively violent under unsuitable physical conditions. The general mechanism has been discussed [3], The explosion hazards associated with the use of acidic catalysts to polymerise furfuryl alcohol may be avoided by using as catalyst the condensation product of 1,3-phenylenediamine and 1-chloro-2,3-epoxypropane [4]. [Pg.704]

Chloro-2,3-epoxypropane See 1 -Chloro-2,3-epoxypropane Sulfuric acid... [Pg.1714]

Ml - PHENOL, 4,4 -ISOPROPYLIOENEOI-, polyeier with 1 -CHLORO-2.3-EPOXYPROPANE... [Pg.157]

A mixture of 18.0 g (0.12 mole) 7-hydroxyphthalide, 180.0 g of l-chloro-2,3-epoxypropane (2 moles) and 0.5 ml of piperidine is heated at 100°C for about 5 h and then the unreacted 1-chloro-2,3-epoxypropane is distilled off in vacuum to yield 12.0 g (48%) of 7-(2,3-epoxypropoxy)phthalide, melting point 88°-90°C, (crystallized successively from methanol and ethyl acetate). [Pg.115]

See other pages where 1- Chloro-2,3-epoxypropane, is mentioned: [Pg.451]    [Pg.468]    [Pg.676]    [Pg.92]    [Pg.203]    [Pg.335]    [Pg.344]    [Pg.366]    [Pg.367]    [Pg.1309]    [Pg.113]    [Pg.241]    [Pg.242]    [Pg.121]    [Pg.335]    [Pg.344]    [Pg.366]    [Pg.367]    [Pg.673]    [Pg.248]    [Pg.249]    [Pg.768]    [Pg.523]    [Pg.386]    [Pg.34]    [Pg.1203]    [Pg.971]    [Pg.519]    [Pg.630]    [Pg.848]    [Pg.2027]    [Pg.127]    [Pg.587]   
See also in sourсe #XX -- [ Pg.294 ]

See also in sourсe #XX -- [ Pg.2 , Pg.15 ]



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1 2 Epoxypropane

F l-Chloro-2,3-epoxypropane

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