Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mei-Li Feng"'
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 7, Pp o1806-o1806 (2010)
The asymmetric unit of the title compound, C8H8Br2O2, contains one half-molecule, the complete molecule being generated by inversion symmetry.
Externí odkaz:
https://doaj.org/article/8d1a22260c5f49b3b3dddb3f2c06c763
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 6, Pp o1487-o1487 (2010)
In the title salt, C5H14NO+·C2F3O2−, the cation and anion are linked by N—H...O and O—H...N hydrogen bonds, generating a three-dimensional network.
Externí odkaz:
https://doaj.org/article/5dab2545affa4617a20431335abd3c15
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 4, Pp o785-o785 (2010)
The molecular structure of the title compound, C9H10N6, exhibits four cyanomethyl groups around a central N—CH2—N unit. In the crystal structure, molecules are connected via intermolecular C—H...N hydrogen bonds, forming a three-dimensional net
Externí odkaz:
https://doaj.org/article/14f9097388ee41f9a1e08544a9d5cb2e
Publikováno v:
Acta Crystallographica Section E, Vol 64, Iss 7, Pp o1281-o1281 (2008)
The dihydrofuran ring of the title compound, C9H9NO3, adopts an envelope conformation. The nitro group is twisted slightly away from the attached benzene ring [dihedral angle = 21.9 (1)°].
Externí odkaz:
https://doaj.org/article/e306faecfaa34ec1841b9d587989287c
Autor:
Mei-Li Feng, 馮玫麗
92
Currently global shipping industry has from grew stage advance to mature period. The container ship capacity of supply exceeds the demand and the economy depression impacted traditional industry fiercely more competitors join the market cause
Currently global shipping industry has from grew stage advance to mature period. The container ship capacity of supply exceeds the demand and the economy depression impacted traditional industry fiercely more competitors join the market cause
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/50415293932339461663
Akademický článek
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Publikováno v:
Pest Management Science. 68:986-994
BACKGROUND: Phthalic acid diamide derivatives are among the most important classes of synthetic insecticides. In this study, a 3,3-dichloro-2-propenyloxy group, the essential active group of pyridalyl derivatives, was incorporated into phthalic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::662682d94189467ffe5a241814d1c62c
https://doi.org/10.1002/ps.3243
https://doi.org/10.1002/ps.3243
Publikováno v:
Journal of Agricultural and Food Chemistry. 58:10999-11006
Phthalic acid diamides have received considerable interest in agricultural chemistry due to a novel action mode, extremely high activity against a broad spectrum of lepidopterous insects, low acute toxicity to mammals, and environmentally benign char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d22ddc5c5b7cd6e456af16f5187dff66
https://doi.org/10.1021/jf1021708
https://doi.org/10.1021/jf1021708
Publikováno v:
Pest management science. 68(7)
Phthalic acid diamide derivatives are among the most important classes of synthetic insecticides. In this study, a 3,3-dichloro-2-propenyloxy group, the essential active group of pyridalyl derivatives, was incorporated into phthalic acid diamide deri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7311ea4deb22122fc105ed8faa308134
https://pubmed.ncbi.nlm.nih.gov/22555940
https://pubmed.ncbi.nlm.nih.gov/22555940
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 66, Iss 4, Pp o785-o785 (2010)
Acta Crystallographica Section E, Vol 66, Iss 4, Pp o785-o785 (2010)
The molecular structure of the title compound, C9H10N6, exhibits four cyanomethyl groups around a central N—CH2—N unit. In the crystal structure, molecules are connected via intermolecular C—H...N hydrogen bonds, forming a three-dimensional net
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9aaa38b2e865dcc07cd7a818aab2b4f
https://pubmed.ncbi.nlm.nih.gov/21580624
https://pubmed.ncbi.nlm.nih.gov/21580624