摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-hydroxyethyl 5-(2-chloro-4-trifluoromethyl phenoxy)-2-nitrobenzoate | 77207-06-8

中文名称
——
中文别名
——
英文名称
2-hydroxyethyl 5-(2-chloro-4-trifluoromethyl phenoxy)-2-nitrobenzoate
英文别名
2-Hydroxyethyl-5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate;2-hydroxyethyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate;[2-Hydroxyethyl]5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate;2-hydroxyethyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate
2-hydroxyethyl 5-(2-chloro-4-trifluoromethyl phenoxy)-2-nitrobenzoate化学式
CAS
77207-06-8
化学式
C16H11ClF3NO6
mdl
——
分子量
405.715
InChiKey
GSJYIZFLSJSZLO-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    464.6±45.0 °C(Predicted)
  • 密度:
    1.506±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    102
  • 氢给体数:
    1
  • 氢受体数:
    9

SDS

SDS:57322b0ec22913a33d7ec4da82817eb7
查看

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Substituted diphenyl ether herbicides and process for use
    申请人:GAF Corporation
    公开号:US04429146A1
    公开(公告)日:1984-01-31
    This invention relates to substituted diphenyl ethers having selective herbicidal properties and having the formula: ##STR1## wherein R is a saturated or unsaturated, straight chain or branched aliphatic hydrocarbon radical of from 1 to 18 carbon atoms wherein one or more of the --CH.sub.2 -- groups can be replaced with --O--, --S--, --S--S--, --SO--, --SO.sub.2 -- or --NR.sub.2 -- and said hydrocarbon radical is optionally substituted with halogen, trihalomethyl, cyano, aryl, hydroxy, alkoxy, nitro or cycloalkyl having 3 to 6 carbon atoms; R.sub.1 is ##STR2## R.sub.3 is ##STR3## R.sub.2 is hydrogen or a saturated or unsaturated straight or branched chain aliphatic radical having from 1 to 8 carbon atoms, optionally substituted with halogen, hydroxy, alkoxy, cyano or nitro; R.sub.4 and R.sub.5 are independently a saturated or unsaturated, straight or branched chain aliphatic radical having 1 to 8 carbon atoms optionally substituted with halogen, trihalomethyl, alkoxy or cyano; hydrogen or phenyl optionally substituted with halogen, alkyl, alkoxy, trihalomethyl, nitro or cyano; R.sub.6 is a saturated or unsaturated straight chain or branched aliphatic radical containing from 1 to 8 carbon atoms, optionally substituted with halogen, trihalomethyl, cyano, hydroxy, nitro, acetoxy, alkoxy, thioalkoxy or aryl; an aryl radical optionally substituted with halogen, trihalomethyl, hydroxy, cyano, nitro, alkyl or alkoxy; a cyclic 3-6 membered ring alkylene or 5-6 membered ring alkenylene or benzyl optionally substituted with halogen, trihalomethyl, alkyl, hydroxy, alkoxy or cyano; R.sub.7 is an alkylene diradical having from 1 to 6 carbon atoms; X and X' are each independently --O--, --S-- or --NR.sub.2 -- L, M and N are each independently hydrogen, hydroxy, halogen, trihalomethyl, nitro, cyano, alkyl or alkoxy having from 1 to 4 carbon atoms and ##STR4## m has a value of from 1 to 6 and n in each instance has a value of from 0 to 1.
    这项发明涉及具有选择性除草特性的取代二苯醚,其化学式为:其中R是具有1至18个碳原子的饱和或不饱和、直链或支链脂肪烃基,其中一个或多个--CH.sub.2--基团可以被--O--、--S--、--S--S--、--SO--、--SO.sub.2--或--NR.sub.2--取代,且该烃基可以选择性地被卤素、三卤甲基、氰基、芳基、羟基、烷氧基、硝基或具有3至6个碳原子的环烷基取代;R.sub.1是;R.sub.3是;R.sub.2是氢或具有1至8个碳原子的饱和或不饱和、直链或支链脂肪基,可以选择性地被卤素、羟基、烷氧基、氰基或硝基取代;R.sub.4和R.sub.5分别是具有1至8个碳原子的饱和或不饱和、直链或支链脂肪基,可以选择性地被卤素、三卤甲基、烷氧基或氰基取代;氢或苯基,可以选择性地被卤素、烷基、烷氧基、三卤甲基、硝基或氰基取代;R.sub.6是具有1至8个碳原子的饱和或不饱和直链或支链脂肪基,可以选择性地被卤素、三卤甲基、氰基、羟基、硝基、乙酰氧基、烷氧基、硫代烷氧基或芳基取代;一种芳基,可以选择性地被卤素、三卤甲基、羟基、氰基、硝基、烷基或烷氧基取代;一个环状3-6成员环烷基或5-6成员环烯基或苄基,可以选择性地被卤素、三卤甲基、烷基、羟基、烷氧基或氰基取代;R.sub.7是具有1至6个碳原子的烷基二基;X和X'各自独立地是--O--、--S--或--NR.sub.2--;L、M和N各自独立地是氢、羟基、卤素、三卤甲基、硝基、氰基、具有1至4个碳原子的烷基或烷氧基;m的值为1至6,每种情况下n的值为0至1。
  • Selective process for the preparation of hydroxy alkyl phenoxy benzoates
    申请人:GAF Corporation
    公开号:US04448982A1
    公开(公告)日:1984-05-15
    This invention relates to a process for the preparation of hydroxy alkyl phenoxy benzoates in a purified state involving the reaction of ethylene or propylene carbonate and a phenoxy benzoic acid having the formula ##STR1## wherein X is O or S; G is selected from the group of nitro, halo, cyano or a hydrogen atom; L, M and N are independently selected from the group of halo, trihaloalkyl, lower alkyl, lower alkoxy and nitro or a hydrogen atom at a temperature within the range of from 90.degree. C. to 125.degree. C.
    这项发明涉及一种制备羟基烷基酚基苯甲酸酯的纯化方法,涉及乙烯或丙烯碳酸酯与具有以下结构式的苯甲酸酯反应:其中X为O或S;G选自硝基、卤素、氰基或氢原子;L、M和N独立选自卤素、三卤代烷基、低级烷基、低级烷氧基和硝基或氢原子,反应温度在90°C至125°C范围内。
  • Process for the preparation of substituted diphenyl ethers
    申请人:GAF Corporation
    公开号:US04797505A1
    公开(公告)日:1989-01-10
    This invention relates to certain phenoxybenzoates having excellent selective herbicidal properties. The compounds of the present invention are defined by the formula ##STR1## wherein L, M and N are independently hydrogen, halogen, trihalomethyl, nitro, cyano, C.sub.1-4 alkyl, C.sub.1-4 alkoxy and ##STR2## and A is selected from the group of radicals defined by the formulae: ##STR3##
    本发明涉及某些具有优异选择性除草性能的苯氧基苯甲酸酯。本发明的化合物由以下公式定义:##STR1## 其中L、M和N分别是氢、卤素、三卤甲基、硝基、氰基、C.sub.1-4烷基、C.sub.1-4烷氧基和##STR2##,而A是从以下公式定义的基团组中选择的:##STR3##
  • New phenoxybenzoates, process for preparing these compounds, compositions containing them and method of use
    申请人:GAF CORPORATION
    公开号:EP0066106A1
    公开(公告)日:1982-12-08
    This invention relates to new phenoxybenzoates having high pre- and post- emergence herbicidal activity against indicator weeds; and are particularly effective against broadleaf weeds, such as morning glory. In addition to such effective herbicidal activity, they exhibit an unusual selectivity against important agromonic crops, such as cotton, rice, soybean, corn, wheat and sorghum.
    本发明涉及新型苯氧基苯甲酸酯,对指示性杂草具有很高的出苗前和出苗后除草活性;对阔叶杂草(如牵牛花)特别有效。除了这种有效的除草活性外,它们还对重要的农作物,如棉花、水稻、大豆、玉米、小麦和高粱表现出不同寻常的选择性。
  • BROWN, MICHAEL J.;LIU, KOU-CHANG
    作者:BROWN, MICHAEL J.、LIU, KOU-CHANG
    DOI:——
    日期:——
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐