Results 131 to 140 of about 974 (165)

Enzyme from Soil Bacterium Hydrolyzes Phenylcarbamate Herbicides

Science, 1965
An enzyme preparation from Pseudomonas sp., isolated from a soil culture by an enrichment technique, liberated 3-chloroaniline from the herbicide isopropyl N -(3-chlorophenyl) carbamate. Aniline, 3-chloroaniline, and 3,4-dichloroaniline were detected when the enzyme preparation was incubated ...
P C, Kearney, D D, Kaufman
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ChemInform Abstract: Microbial Oxygenation of Cycloheptyl‐N‐phenylcarbamate and (.+‐.)‐trans‐2‐Fluorocycloheptyl‐N‐phenylcarbamate with Beauveria bassiana.

ChemInform, 1998
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
S. PIETZ, R. FROEHLICH, G. HAUFE
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[Antimycobacterial effects of pyrrolidinoethylester alkoxysubstituted phenylcarbamic acids].

Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti, 2002
Pyrrolidinoethylesters of alkoxysubstituted phenylcarbamic acids, formerly investigated for local anaesthetic activity, can be considered to be potential antituberculotics. They are effective in vitro against Mycobacterium tuberculosis, Mycobacterium kansasii, and Mycobacterium avium.
K, Waisser, J, Cizmárik, K, Drazková, J, Kaustová   +3 more
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Inhibition of Growth of Apical Meristems by Ethyl Phenylcarbamate

Nature, 1950
Templeman and Sexton1 were the first to show that ethyl and isopropyl phenylcarbamates were selectively toxic to higher plants and therefore potentially valuable as herbicides. Since then, Ennis2, Ivens and Blackman3 and Doxey4 have reported on the mitotic effects induced by these compounds.
G W, IVENS, G E, BLACKMAN
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ChemInform Abstract: PHOTOREARRANGEMENT REACTIONS OF METHYL PHENYLCARBAMATE

Chemischer Informationsdienst, 1976
AbstractBei der Bestrahlung von Phenylmethylcarbamat (I) unter Sauerstoff entstehen im ersten Schritt die intramolekularen Umlagerungsprodukte (II) und (III), die Bildung von Anilin wird nicht beobachtet.
Y. TAKANAKA, T. YAMAGATA, T. ISHII, T. HANDA   +3 more
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Molecular Structure and Liquid-Crystalline Characteristics of Chitosan Phenylcarbamate

Biomacromolecules, 2008
Chitosan phenylcarbamate (CtsPC) samples were synthesized to have different degrees of substitution (DS) ranging from approximately 2.7 to approximately 3.7, and the lyotropic liquid crystallinity was mainly characterized by spectrophotometry. The products of DS>2.8 formed a cholesteric type of mesophase in concentrated solutions of >44 wt % with polar
Yasunori, Kuse, Daisuke, Asahina, Yoshiyuki, Nishio   +2 more
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ChemInform Abstract: Nitration of Alkyl N‐Phenylcarbamates.

ChemInform, 1993
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
A. V. VELIKORODOV, T. N. MAKSIMOVA, V. B. MOCHALIN   +2 more
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Chromosome Contraction byo-Isopropyl-N-Phenylcarbamate (IPC)

Stain Technology, 1967
A selective herbicide IPC (o-isopropyl-N-phenlycarbamate) causes contraction of chromosomes in the prophase, metaphase, and anaphase stages of mitosis in cells of treated root tips. Effective concentrations in aqueous solution lie between 2.5 and 50 ppm, and effective times between 1 and 4 hr, depending upon the species of plant.
W B, Storey, J D, Mann
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Acid catalysed condensation of methyl N-phenylcarbamate

Applied Catalysis, 1990
Abstract The condensation of methyl N-phenylcarbamate with formaldehyde to methylene diphenyl diurethane has been studied in the presence of various liquid and solid acid catalysts in a batch reactor. The 50% sulphuric acid and Amberlyst 15 were found to be the best liquid and solid catalysts, respectively.
LEE, Chul W., LEE, Sang M., PARK, Tae K., PARK, Kwang H., Lee, Jae Sung   +4 more
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Antimycobacterial activity of piperidinylpropyl esters of alkoxy-substituted phenylcarbamic acids

Folia Microbiologica, 2003
A series of 17 hydrochlorides of piperidinylpropyl esters of alkoxy-substituted phenylcarbamic acids with the alkoxy group in position 2, 3 or 4 on the phenyl ring, and basic substituents attached to the moiety in position 3, were evaluated for in vitro antimycobacterial activity against the strains of Mycobacterium tuberculosis, M.
K, Waisser, K, Drazková, J, Cizmárik, J, Kaustová   +3 more
openaire   +2 more sources