Pentyl 1-Phenyl-butyl -propyl

Anilino-propyl)-methyl- E2, 143 (2-Arylaminocarbonyl-alkyl)-organo- E2, 140 (a-Bcnzylamino-benzyI)-ethyI- E2, 131 ( -Benzylamino-benzyl)-phenyl- E2, 131 (l-Benzylamino-eihyl)-phenyl- E2, 131 (l-Benzylamino-pentyl)-phenyl- E2, 131 Benzyl-butyl- -ethylester XII/1, 255 [(Bcnzyl-carboxymethyl-amino)-methyl]-ethyl- ... 

Phenyl-butyl-(2)]-1-athoxycarbonyl- 245 fl-Phenyl-butyliden-(3)]- 241 2-[3-Phenyl-butyliden-(2)]-1-athoxycarbonyl- 245 2-[3-Phenyl-pentyl-(3)]-l-pentyliden-(3)- 242 (2-Phenyl-propyl)- 241 [l-Pheny -propyl-(2)J- 242 (2-Phenyl-propyliden)- 241 [l-Phenyl-propyliden-(2)]- 242 2-(2-Phenyl-propyl-(2)]-l-isopropyliden- 243 Propyliden- 592... 

Butyloxy-propyl- XII/1, 257 Butyloxy-trimelhylsilyloxy- El, 339 tert.-Butyl-phenyl- El, 241, 244 tcrt.-Butyl-phcnyl-trifluoracetyl- E2, 8 (tti-Carboxy-alkyl)-diphenyl- E2, 52, 53 (a-Carboxy-bcnzyl)-diphenyl- E2, 34 (lO-Carboxy-decyl)-diphenyl- E2, 53 (2-Carboxy-ethyl)-diphenyl- Xll/1, 146 Carboxymethyl-diphcnyl- XII/1, 148 E2, 65, 66 (S-Carboxy-pentyl)-diphenyl- E2, 53 (3-Carboxy-phenyl)-diphenyl- XII/1, 143 El, 167 (4-Chlor-benzyl)-diphenyl- E2, 16, 18 (a-Chlor-benzyl)-diphenyl- E2, 11, 23 Chlorethinyl-diphenyl- E2, 23, 23 Chlor-ethoxy- El, 321 (2-Chlor-elhoxy)-ethyl- E2, 187 (2-Chlor-eihoxy)-hydroxy- XII/2, 11 Ammoniumsalz... 

X = N, P R = phenyl, -propyl, -butyl, -pentyl) is required for charge balance... 

Y = n-butyl, n-propyl, n-pentyl, (l-methyl)butyl, cyclohexyl, benzyl, phenyl, (2-hydroxy)ethyl, (2-dimethylamino)ethyl... 

The R group methyl, ethyl, propyl, butyl, pentyl, vinyl, or phenyl (Scheme 1) influences the hydrolysis rate of the silane endcapping group. The size and the inductive effect of the substituents R, acetyl, methyl, ethyl, or imine modify the reactivity as well. 

This list is exhaustive as far as non-carbon parent hydrides are concerned. A number of established shortened or entirely non-systematic names are also used for carbon-based hydrides methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclohexyl, phenyl, naphthyl, etc. 

The abbreviations used for chemical substituents are as follows Me-methyl, Et-ethyl, Pr-propyl, Bu-butyl, Pen-pentyl, Hex-hexyl, Hept-heptyl, Ph-phenyl, u-normal, i-iso, sec-secondary, t-tertiary, and c-cyclo. 

A thyl-( 2-methyl-propyl)-piperidyl-( 3)- 2 60 (2-Amino-athyl)-butyl-(2)-cyclopentyl- 132 (2-Amino-athyl)-(2-dimethylamino-athyl)- 132 (2-Amino-athyl)-(3-dimcthylamino-propyl)- 132 (2-Amino-athyl)-(2-piperidino-athyl)- 132 (2-Amino-athyl)-(3-piperidino-propyl)- 132 (2-Amino-athyl)-propyl-butyl-(2)- 132 (2-Amino-athyl)-propyl-pentyl-(2 bzw. 3)- 132 (2-Amino-ben7yl)-benzyliden- 230 (4-Amino-phenyl)-(4-ch or-benzyliden)- 224 Aryl- 742ff. 

Dimethylamino-athyl)-benzyliden- 230 Dimethyl-(4-amino-butyl)- 122 Dimethyl-(3-amino-pentyl)- 122 Dimethyl-cyclohexyl- 631 Dimethyl-hexadecyl- 426 Dimethyl-(2-nitro-propyl)- 491 Dimethyl-phenyl- 631 Dimethyl-) 2-vinyl-benzyl)- 675 Dinonyl- 41 4 Dipentyl-(3)- 442 Diphenyl- 25, 54, 576 Diphenylmethyl- 25, 671, 690 Diphenylmethyl-phenyl-... 

The following abbreviations have been used for substituents Me = methyl Et = ethyl Pr = propyl Bu = butyl Pent = pentyl Hex = hexyl Oct = octyl Ph = phenyl Ac = acetyl apio/ = apio-furanoside galp = galacto-pyranoside glcp = gluco-pyranoside rhamps rhamno-pyranosyl, xylp = xylo-pyranosyl. 

A chemical substance or ion is generally referred to in the text by its name or formula, but in tables and as subscripts, abbreviations are generally employed. The common abbreviations of alkyl chains employed are as follows Me, methyl Et, ethyl Pr, 1-propyl Bu, 1-butyl Pe, 1-pentyl Hx, 1-hexyl Oc, 1-octyl and Ph, phenyl. Common solvents have the following abbreviations EG, 1,2-ethanediol THE, tetrahydrofuran Diox, 1,4-dioxane PC, propylene carbonate FA, formamide DMF, A,A-dimethylfonnamide NMPy, A-methyl-2-pyrrolidinone Py, pyridine DMSO, dimethylsulfoxide TMS, tetramethylenesulfone (sulfolane), and HMPT, hexamethyl phosphoric triamide. The names of other solvents are occasionally abbreviated as noted in the footnotes of tables. 

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