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CH2

A propagation step involving growth around an active center follows RCH2—CHCl -h CH2=CHC1 —> RCH2—CHCl—CH2—CHCl and so on, leading to molecules of the structure... [Pg.21]

R-CHCl—CHCl—CH2—(CHCl—CH2L—R... [Pg.22]

H2N(CH2)jCOOH, C H,3N02. Prepared from -benzoylaminocapronitrile or from l-hydroxycyclohexylhydroperoxide, m.p. 205 0. Aminocaproic acid is an antifibrinolytic agent, used to treat thrombosis in the deep veins. amiDoethyl alcohol. See ethanolamines. [Pg.29]

CH3-[CH2],8-C00H. M.p. 75 C. A fatty acid occurring as glycerides in peanut and other vegetable oils. [Pg.40]

HOOO(CH2)7COOH. Colourless plates, m.p. lOfi C. Made by the oxidation of oleic acid with ozones. [Pg.47]

Butene, a-bulylene, CH3CH2CH CH2-Prepared by passing the vapour of 1-butanol over heated alumina. [Pg.72]

Melbylpropene, isobutylene, isobutene, Me2C CH2 Prepared by heating r-butanol with oxalic acid. [Pg.72]

H2N (CH2]5 NH2. a syrupy fuming liquid, b.p. 178-180 - C. Soluble in water and alcohol. Cadaverine is one of the ptomaines and is found, associated with pulrescine, in putrefying tissues, being formed by bacterial action from the amino-acid lysine. It is found in the urine in some cases of the congenital disease cystinuria. The free base is poisonous, but its salts are not. [Pg.74]

See other pages where CH2 is mentioned: [Pg.304]    [Pg.19]    [Pg.19]    [Pg.19]    [Pg.19]    [Pg.19]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.22]    [Pg.22]    [Pg.49]    [Pg.50]    [Pg.51]    [Pg.118]    [Pg.118]    [Pg.13]    [Pg.18]    [Pg.19]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.23]    [Pg.28]    [Pg.30]    [Pg.32]    [Pg.40]    [Pg.41]    [Pg.48]    [Pg.48]    [Pg.53]    [Pg.60]    [Pg.68]    [Pg.70]    [Pg.70]    [Pg.71]    [Pg.72]    [Pg.73]    [Pg.78]    [Pg.78]   
See also in sourсe #XX -- [ Pg.780 ]

See also in sourсe #XX -- [ Pg.2 , Pg.66 ]

See also in sourсe #XX -- [ Pg.2 , Pg.219 ]

See also in sourсe #XX -- [ Pg.6 , Pg.7 , Pg.8 , Pg.8 , Pg.9 ]

See also in sourсe #XX -- [ Pg.11 ]



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A R(CO)CH2 Umpolung Equivalent

Alkanes Containing the CH3 and CH2 Units

C2H5CH=CH2

CH2 radical

CH2 reactions

CH2 units

CH2, dimerization

CH2-CH-COOH

CH2-groups

CH2=CH (ONO

CH2=CHCCH

CH2=CHCHO

CH2=CHCN

CH2— (active methylene) — —CF2— (difluoromethylene)

CH3Y/CH2 = Y- systems

Ch2 domain

Ethylene glycol [CH2

FID Manipulation FT, EM, SINE BELL (CH2 Signal of

Molecular rings, made of CH2 fragments

Mono-Substituted Cyclic Alkanes ZCR(CH2)n

Reaction of (Cl2Si—CH2)3 with KFe(CO)2cp

Reactions of (H2Si—CH2)3 with Co2(CO)

Reactions of CH2 with

Syntheses via Metallation of CH2 or CH Groups

The Formation of CH2-Linked 1,3,5,7-Tetrasilaadamantanes

The Localized Orbitals of a CH2 Group

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