Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | a | b | c | d | e | f | g | h | i | j | k | l | m | n | o | p | q | r | s | t | u | v | w | x | y | z

|< << >> > |

Cytotoxicity towards A2780, A2780cisR, HT29 and A549 cancer cells, and ECRF24 endothelial cells, and intracellular uptake in A2780 cells and logP0 w values of 1 - 3. Errors represent the standard error of the mean

Cytotoxicity trypsin inhibitors from grain wheat

Cytotoxity of C-10-Modified Taxoids a

Cytotoxity of selected podophyllotoxin derivatives against KB cells and cellular protein-linked DNA breaks

Czechoslovak standards for potassium hydroxide

Czechoslovak standards for sodium hydroxide

Czechoslovakian permitted explosives

C—C and C—H Bond Lengths and Bond Strengths in Alkynes, Alkenes, and Alkanes

C—C ring stretching force constants for tri-x-substituted cyclopropenium, ions

C—F bond distances in the fluorobenzenes

C—H and 0—H Acidities of Some Representative Compounds3

C—H bond activation of aldehydes using Nai2 Cp Ir.

C—H Bond Energies

C—H bond insertion of 1,3,5-cycloheptatriene reported by Davies.

C—H bond insertion of acyclic silyl enol ethers reported by Davies.

C—H bond insertion of cyclic silyl enol ethers reported by Davies.

C—H bond insertion reactions of 1-substituted cyclohexene reported by Davies.

C—N Rotational barriers of substituted aminoalkyl radicals H2NCHR.a

C—N Rotational barriers of substituted aminoalkyl radicals HjNCHR.

C—N Stretch of Primary, Secondary, and Tertiary Aromatic Amines

C—S and S—S bond energies upper limits e V

C—X bond dissociation energies of halogenoethanes

D analytical models

D and 2.5-D floorplans for Category 2 designs

D and O parameters of various acids and bases, taken from Ref.

|< << >> > |

SEARCH

© 2024 chempedia.info