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CH3CH

Buiene, -butylene, CH3CH CHCH3-Prepared by heating 2-buianol with sulphuric acid. It occurs as two geometrical isomers. [Pg.72]

Dihydroxybutane. -butylene glycol, CH3CH(0H)CH2CH20H, b.p. 204°C. Manufactured by reduction of aldol or by the action of yeast on aldol. Used to prepare butadiene. Used in brake fluids, in gelling agents and as an intermediate in plasticizers. [Pg.72]

CH3CH(0H)C(0)0Et. A colourless liquid with a pleasant odour, b.p. 154 C. Manufactured by distilling a mixture of ( )-lactic acid, ethanol and benzene in the presence of a little sulphuric or benzenesulphonic acid. It is a solvent for cellulose nitrate and acetate and also for various resins. Used as a lacquer solvent. [Pg.169]

Besides specifications on atoms, bonds, branches, and ring closure, SLN additionally provides information on attributes of atoms and bonds, such as charge or stereochemistry. These are also indicated in square [ ] or angle < > brackets behind the entity e.g., trans-butane CH3CH=[s=t]CHCH3). Furthermore, macro atoms allow the shorthand specification of groups of atoms such as amino adds, e.g., Ala, Protein2, etc. A detailed description of these specifications and also specifications for 2D substructure queries or combinatorial libraries can be found in the literature [26]. [Pg.29]

I the glucosides are similar in chemical nature j to the acetals, e.g, CH3CH(OC2Hs)2, which... [Pg.143]

Mono and Di-iubstitution Derivatives. The enolic sodium derivative of ethyl acetoacetate (E) is prepared by mixing ethanolic solutions of the ester and of sodium ethoxide. It should not be prepared by the direct action of metallic sodium on the ester, as the reaction is slow and the nascent hydrogen evolved reduces some of the ester to ethyl p4iydroxy- butyrate, CH3CH(OH)CHjCOOEt. [Pg.269]

Alcohols containing the CH3CH(OH) group give the iodoform... [Pg.335]

CH3CH=CHCHO-1-HjC(COjH)2 CH3CH=CHCH=CHCOjH-1-COj-1-HjO... [Pg.466]

MC.-Octyl alcohol methyl n-hexyl carbinol CH3CH(OH)(CHj)jCH3 = CgH,OH is converted by heating with phthalic anhydride into sec.-octyl hydrogen phthalate ... [Pg.505]

Stem Nucleus CH3CH3CH3 CHaCHj and CH, CH3CH, CHjCHjCH,... [Pg.1115]


See other pages where CH3CH is mentioned: [Pg.71]    [Pg.72]    [Pg.116]    [Pg.168]    [Pg.262]    [Pg.330]    [Pg.366]    [Pg.136]    [Pg.73]    [Pg.77]    [Pg.77]    [Pg.77]    [Pg.93]    [Pg.121]    [Pg.224]    [Pg.331]    [Pg.351]    [Pg.324]    [Pg.325]    [Pg.247]    [Pg.247]    [Pg.302]    [Pg.318]    [Pg.319]    [Pg.320]    [Pg.320]    [Pg.332]    [Pg.335]    [Pg.351]    [Pg.351]    [Pg.381]    [Pg.381]    [Pg.427]    [Pg.460]    [Pg.464]    [Pg.464]    [Pg.831]    [Pg.882]    [Pg.926]    [Pg.194]    [Pg.47]   
See also in sourсe #XX -- [ Pg.247 , Pg.253 ]




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CH3CH COOH

CH3CH, reaction

CH3CH=CHCOOH

The Ethyl Group (CH3CH

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