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Alcohol propenyl

Glycerol -dichlorohydrin, 2.3-dichloro-propanol, CH2CI CHC1 CH2 0H. Colourless liquid, b.p. 182 C. Prepared by the chlorination of propenyl alcohol. Oxidized by nitric acid to 1,2-dichloropropionic acid. Reacts with NaOH to give epichlorohydrin. [Pg.192]

As propylene oxide is introduced into the reactor, a portion of it is converted to allyl alcohol and propenyl alcohol via a rearrangement [5] ... [Pg.766]

Synonyms AA AI3-14312 Allyl al Allylic alcohol BRN 0605307 Caswell No. 026 CCRIS 747 EINECS 203-470-7 EPA pesticide chemical code 068401 3-Hydroxypropene 3-Hydroxy-propylene NSC 6526 Orvinyl carbinol Propenol Propenol-3 Propen-l-ol-3 l-Propenol-3 1-Propen-3-ol 2-Propenol 2-Propen-l-ol Propenyl alcohol 2-Propenyl alcohol RCRA waste number P005 UN 1098 Vinyl carbinol Weed drench. [Pg.87]

Propenol, see Allyl alcohol 2-Propen-l -ol, see Allyl alcohol Propenol-3, see Allyl alcohol 2-Propen-l -one, see Acrolein Propenonitrile, see Acrylonitrile Propenyl alcohol, see Allyl alcohol 2-Propenyl alcohol, see Allyl alcohol... [Pg.1506]

Allyl Alcohol (Vinyl Carbinol, Propenyl Alcohol, 2-Propeno-1, Propenol-3)... [Pg.227]

Synonyms and trade names vinyl carbinol, propenyl alcohol, 2-propeno-l, propenol-3... [Pg.48]

ALCOHOL 2-PROPENYL ALCOHOL RCRA WASTE NUMBER POOS SHELL UNDRAUTTED A VINYLCARBINOL XX EED DRENCH... [Pg.37]

PROPENYLACRYLIC ACID see SKUOOO PROPENYL ALCOHOL see AF "500 2-PROPENYL ALCOHOL see AFV500... [Pg.1854]

AI3-14312 Alcool allilco Alcool allylique Allilowy alkohol Allyl alcohol Allylalkohol Allyllc alcohol Caswell No. 026 CCRIS 747 EINECS 203469-1 EPA PesScide Chemical Code 068401 HSDB 192 3-Hydroxypropene NSC 6526 2-Propenol 2-Propen-1-ol Propen-1-ol-3 Prapenyl alcohol 2-Propenyl alcohol RCRA waste number POOS Shell unkrautted A UN10M Vinyl carbinol Weed drench. Intermediate for pharmaceuticals and other organic chemicals, herbicide. Liquid mp = -129° bp = 97° d = 0.8640 XmKs = 273 nm (s = 4677, H2SO4) freely soluble in H2O, EtOH, Et20, soluble in CHCI3 LDso (rat ort) = 64 mg/kg. [Pg.19]

Allyl alcohol propen-l-ol-3,propenyl alcohol CH2 CHCH20H 58-08 col- Iq- 0-854 -129 96.6 CO CO CO... [Pg.76]

Prior hydrolysis of the difluoromethylene group in either the 3- or 17-cycIo-propenyl alcohols (13Sa and b) affords the corresponding cyclopropenones, which on treatment with the fluoramine reagent are converted cleanly into analogous 3 - and 17/9-allenic carbonyl fluorides (142) and (143) in this case a-isomers were not detected (Scheme 38). [Pg.99]

Synonyms AA Allylic alcohol 3-Hydroxypropene 2-Propene-1-ol Propenol Propen-1-ol-3 1-Propen-3-ol 2-Propen-1-ol Propenyl alcohol 2-Propenyl alcohol Vinylcarbinol... [Pg.157]

Propenyl acetate. See Allyl acetate 2-Propenylacrylic acid. See Sorbic acid Propenyl alcohol 2-Propenyl alcohol. See Allyl... [Pg.3725]

Allyl alcohol (propenyl alcohol, AA, 2-pro-pene-l-ol) n. CH2=CHcCH2-OH. A colorless liquid with a characteristic pungent odor synthesized by hydrolysis of allyl chloride (from propylene) with dilute caustic, or by the dehydration of propylene glycol. It is a basic material for all allyl resins, and its esters are used as plasticizers (See image). [Pg.42]

C3H6O 107-18-6 Prop-2-en-l-ol syn. GAllyl alcohol G2-Propenyl alcohol G2-Propen-l-ol... [Pg.60]

Analysis of Reagent Purity H NMR, IR, elemental analysis. Preparative Methods the title reagent is prepared by the reaction of 2-(methylsulfonyl)-3-phenyl-2-propenyl alcohol and phosgene (eq 1). The alcohol is obtained from the corresponding allylic bromide by formate-catalyzed hydrolysis. The synthesis of the bromide involves the Cu(OAc)2-catalyzed addition of methanesulfonyl chloride to -methylstyrene followed by elimination of hydrogen chloride and subsequent free radical bromination of the methyl group (eq 1). ... [Pg.382]

Anethole l-Methoxy-4-(l-Propenyl)benzene p-Propenylanisole 107-18-6 Allyl Alcohol 2-Propen-l-ol Propenyl Alcohol... [Pg.3482]

Ferric Nitrate Iron (III) Nitrate 2-Ethylhexyl Alcohol Strontium Bromide 107-19-7 Propenyl Alcohol 3-Hydroxy-l-Propyne... [Pg.1668]


See other pages where Alcohol propenyl is mentioned: [Pg.192]    [Pg.766]    [Pg.690]    [Pg.729]    [Pg.729]    [Pg.69]    [Pg.729]    [Pg.57]    [Pg.41]    [Pg.1046]    [Pg.10]    [Pg.14]    [Pg.22]    [Pg.108]    [Pg.28]    [Pg.910]    [Pg.1020]    [Pg.1020]    [Pg.71]    [Pg.355]    [Pg.28]    [Pg.21]    [Pg.107]    [Pg.24]    [Pg.52]    [Pg.60]    [Pg.3445]    [Pg.3479]    [Pg.1641]    [Pg.1664]   
See also in sourсe #XX -- [ Pg.14 ]

See also in sourсe #XX -- [ Pg.40 ]




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3- -2-propenyll

Propenylation

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