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2-Chloro-4-fluoroaniline | CAS:2106-02-7
2-Chloro-4-fluoroaniline
  • 名称:2-氯-4-氟苯胺 | 2-Chloro-4-fluoroaniline
  • CAS号:2106-02-7
  • 别名:2-Chloro-4-fluorobenzenamine
  • 分子式:C6H5ClFN
  • 分子量:145.56
  • EINESC号:218-282-0

产品描述

物理化学性质

沸点 192 ºC
闪点 98 ºC
密度 1.219
折射率 1.553-1.555

安全数据

危险品标志 Xn
危险类别码 R20/21/22;R36/37/38
安全说明书 S26;S36/37/39

SDS

来源 SDS样本
Alfa-Aesar 浏览或下载
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Use of plant cell cultures to study graminicide effects on lipid metabolism.Lindsey J Price et al.Phytochemistry, 63(5), 533-541 (2003-06-18) Trypanosoma brucei: inhibition of acetyl-CoA carboxylase by haloxyfop.Patrick A Vigueira et al.Experimental parasitology, 130(2), 159-165 (2011-11-29) Dominant mutations causing alterations in acetyl-coenzyme A carboxylase confer tolerance to cyclohexanedione and aryloxyphenoxypropionate herbicides in maize.W B Parker et al.Proceedings of the National Academy of Sciences of the United States of America, 87(18), 7175-7179 (1990-09-01) Differential sensitivity of lipid metabolism in monocotyledons to grass-specific herbicides.D Herbert et al.Biochemical Society transactions, 21(2), 183S-183S (1993-05-01) A novel W1999S mutation and non-target site resistance impact on acetyl-CoA carboxylase inhibiting herbicides to varying degrees in a UK Lolium multiflorum population.Shiv Shankhar Kaundun et al.PloS one, 8(2), e58012-e58012 (2013-03-08) Acetyl-CoA carboxylase exerts strong flux control over lipid synthesis in plants.R A Page et al.Biochimica et biophysica acta, 1210(3), 369-372 (1994-01-20) Characterisation of target-site resistance to ACCase-inhibiting herbicides in the weed Alopecurus myosuroides (black-grass).Stephen R Moss et al.Pest management science, 59(2), 190-201 (2003-02-18) [Determination of tin compounds in the atmosphere by inversion volt-amperometry].E M Roĭzenblat et al.Gigiena i sanitariia, (4)(4), 62-63 (1986-04-01) An isoleucine-leucine substitution in chloroplastic acetyl-CoA carboxylase from green foxtail (Setaria viridis L. Beauv.) is responsible for resistance to the cyclohexanedione herbicide sethoxydim.Christophe Délye et al.Planta, 214(3), 421-427 (2002-02-22) Inhibition of ACCase220 and ACCase240 isozymes from sethoxydim-resistant and -susceptible maize hybrids.B J Incledon et al.Journal of agricultural and food chemistry, 47(1), 299-304 (1999-11-24) Cellular membranes, the sites for the antifungal activity of the herbicide sethoxydim.B S Pakdaman et al.Pakistan journal of biological sciences : PJBS, 10(15), 2480-2484 (2007-08-01) Genome sequence of foxtail millet (Setaria italica) provides insights into grass evolution and biofuel potential.Gengyun Zhang et al.Nature biotechnology, 30(6), 549-554 (2012-05-15) Rewiring metabolic network by chemical modulator based laboratory evolution doubles lipid production in Crypthecodinium cohnii.Jinjin Diao et al.Metabolic engineering, 51, 88-98 (2018-11-06) Inhibition of 4-hydroxyphenylpyruvate dioxygenase by sethoxydim, a potent inhibitor of acetyl-coenzyme A carboxylase.S Lin et al.Bioorganic & medicinal chemistry letters, 9(4), 551-554 (1999-03-31) In matrix formation of deep eutectic solvent used in liquid phase extraction coupled with solidification of organic droplets dispersive liquid-liquid microextraction; application in determination of some pesticides in milk samples.Abolghasem Jouyban et al.Talanta, 206, 120169-120169 (2019-09-14) Sethoxydim affects lipid synthesis and acetyl-CoA carboxylase activity in soybean.Aicha Belkebir et al.Journal of experimental botany, 57(14), 3553-3562 (2006-09-14) Effects of herbicides on Behr's metalmark butterfly, a surrogate species for the endangered butterfly, Lange's metalmark.John D Stark et al.Environmental pollution (Barking, Essex : 1987), 164, 24-27 (2012-02-09) Inhibition of plant acetyl-coenzyme A carboxylase by the herbicides sethoxydim and haloxyfop.J D Burton et al.Biochemical and biophysical research communications, 148(3), 1039-1044 (1987-11-13) An isoleucine/leucine residue in the carboxyltransferase domain of acetyl-CoA carboxylase is critical for interaction with aryloxyphenoxypropionate and cyclohexanedione inhibitors.O Zagnitko et al.Proceedings of the National Academy of Sciences of the United States of America, 98(12), 6617-6622 (2001-06-07)
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