Results 211 to 220 of about 15,835 (261)
Design, synthesis, and antitumor evaluation of new functionalized spiroindenopyridotriazinepyrans. [PDF]
Safari F, Bayat M, Hosseini H, Homaee A.
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Carcinogenicity of atrazine, alachlor, and vinclozolin. [PDF]
Cattley RC +37 more
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Dalton Trans., 2004
The synthesis of TAS+ C3N3F4- (1) (TAS+ = (Me2N)3S+) and the reactions of 1 with Me3SiOSiMe3 and Me3SiCF3 to give TAS+ C3N3F2O- (2) and TAS+[(NCF)(NCCF3)(NC(CF3)(2)]- (4) are reported. An isomer of 4, TAS+[(NCCF3)2(NCFCF3)]-, compound 6, was obtained by fluoride ion addition to (CF3CN)3.
Melanie, Kingston +3 more
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The synthesis of TAS+ C3N3F4- (1) (TAS+ = (Me2N)3S+) and the reactions of 1 with Me3SiOSiMe3 and Me3SiCF3 to give TAS+ C3N3F2O- (2) and TAS+[(NCF)(NCCF3)(NC(CF3)(2)]- (4) are reported. An isomer of 4, TAS+[(NCCF3)2(NCFCF3)]-, compound 6, was obtained by fluoride ion addition to (CF3CN)3.
Melanie, Kingston +3 more
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2005
Abstract Despite the widespread use of these chemicals, relatively little is known regarding their potential effects on the health of wildlife and humans. In light of such widespread use and limited information about health effects, there has been an in creasing interest in potential detrimental impacts due to unintended exposure ...
Timothy S Gross, R Heath Rauschenberger
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Abstract Despite the widespread use of these chemicals, relatively little is known regarding their potential effects on the health of wildlife and humans. In light of such widespread use and limited information about health effects, there has been an in creasing interest in potential detrimental impacts due to unintended exposure ...
Timothy S Gross, R Heath Rauschenberger
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ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
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AbstractFor Abstract see ChemInform Abstract in Full Text.
C. W. Lindsley, M. E. Layton
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Chromatographic Reviews, 1970
Abstract The major areas of diverse paper, thin-layer, gas and column chromatographic analyses have been reviewed with special emphasis on procedures used for the elaboration of compound homogeneity, metabolism, degradation and mode of action of a variety of 1,3,5-triazines that are of pesticidal, pharmaceutical, chemosterilant and industrial ...
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Abstract The major areas of diverse paper, thin-layer, gas and column chromatographic analyses have been reviewed with special emphasis on procedures used for the elaboration of compound homogeneity, metabolism, degradation and mode of action of a variety of 1,3,5-triazines that are of pesticidal, pharmaceutical, chemosterilant and industrial ...
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2008
[290-87-9] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-4-2-6-3-5-1/h1-3H InChIKey = JIHQDMXYYFUGFV-UHFFFAOYSA-N (C1 electrophile; formylating agent;2 methylenating and aminomethylenating agent;3 in combination with cyclic amines, dehydro-Mannich bases4, 5 are formed) Alternate Name: s-triazine. Physical Data: mp 80–82 °
GIACOMELLI, G, PORCHEDDU, ANDREA, A.
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[290-87-9] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-4-2-6-3-5-1/h1-3H InChIKey = JIHQDMXYYFUGFV-UHFFFAOYSA-N (C1 electrophile; formylating agent;2 methylenating and aminomethylenating agent;3 in combination with cyclic amines, dehydro-Mannich bases4, 5 are formed) Alternate Name: s-triazine. Physical Data: mp 80–82 °
GIACOMELLI, G, PORCHEDDU, ANDREA, A.
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Antimalarials. 3. 1,2,4-Triazines
Journal of Medicinal Chemistry, 1976The syntheses of a number of substituted 1,2,4-triazines as potential antimalarials are described. The structural requirements for antimalarial activity are discussed with reference to the substituents of a phenyl group in the 6 position and amino groups at the 3 and 5 positions.
L C, March +4 more
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