Results 141 to 150 of about 71,285 (330)

Synthesis and Spectroscopic Study of Naphtholic and Phenolic Azo Dyes [PDF]

open access: yes, 2013
Azo dyes are extremely important in variety of industries for variety of technical purposes. Hence, a series of naphtholic azo dyes 1-9 were synthesized via diazotization of substituted aniline derivatives followed by azo coupling with 2-naphthol.
Ajani, Alice O   +4 more
core  

Synthesis of perfluoroalkylene aromatic diamines [PDF]

open access: yes
Analogues of methylene dianilines were synthesized, in which the methylene group between the two aromatic nuclei was replaced by various perfluoroalkylene linkage.
Ito, T. I.   +3 more
core   +1 more source

Iodothiophenes and Related Compounds as Coupling Partners in Copper-Mediated N-Arylation of Anilines

open access: green, 2020
Ghenia Bentabed‐Ababsa   +7 more
openalex   +2 more sources

Nonflammable, antistatic, and heat-sealable film [PDF]

open access: yes
Antistatic, heat-sealable, nonflammable films prepared from polyvinylidene fluoride and polyvinylidene chloride ...
Block, B. P.   +4 more
core   +1 more source

CXVII.—Aniline-black and allied compounds. Part II [PDF]

open access: yesJ. Chem. Soc., Trans., 1912
Arthur George Green   +1 more
openaire   +1 more source

Determination of 14 aniline and benzidine compounds in soil by gas chromatography-mass spectrometry [PDF]

open access: bronze, 2023
Lijuan Wu   +5 more
openalex   +1 more source

Diversity of 3-chloroaniline and 3,4-dichloroaniline degrading bacteria isolated from three different soils and involvement of their plasmids in chloroaniline degradation. [PDF]

open access: yes, 2002
CRUL, Katrien   +7 more
core   +2 more sources

Preparation of organic hydrazides [PDF]

open access: yes, 1959
Thesis (M.A.)--Boston UniversityDue to the actual high price of hydrazine, this chemical cannot be used in an economical preparation of organic hydrazides. A synthesis of such hydrazides can be envisaged by the reduction of N-nitroamides.
Amiel, Jean-Pierre L.
core   +1 more source

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