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(4-amino-3-chlorophenyl)acetic acid | 22106-57-6

中文名称
——
中文别名
——
英文名称
(4-amino-3-chlorophenyl)acetic acid
英文别名
4-amino-3-chlorophenylacetic acid;4-Amino-3-chlorphenylessigsaeure;2-(4-Amino-3-chlorophenyl)acetic acid
(4-amino-3-chlorophenyl)acetic acid化学式
CAS
22106-57-6
化学式
C8H8ClNO2
mdl
——
分子量
185.61
InChiKey
RNPFHSPLVUBKAU-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    63.3
  • 氢给体数:
    2
  • 氢受体数:
    3

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

反应信息

  • 作为反应物:
    描述:
    trans-4-(4-dimethylaminomethylphenyl)-cyclohexanol 、 (4-amino-3-chlorophenyl)acetic acidN,N'-羰基二咪唑 作用下, 生成 trans-O-([4-amino-3-chlorophenyl]acetyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
    参考文献:
    名称:
    O-acyl-4-phenyl-cyclohexanols, their salts, medicaments containing such
    摘要:
    本文描述了通式I的O-酰基-4-苯基环烷醇,其中n表示数字0或1,m表示数字1或2,p表示数字0或1,R.sup.1和R.sup.2分别表示氢、较低的烷基、烯基或炔基,也可以选择性地被取代,或者与它们之间的氮原子一起表示5至7个成员饱和的、单环的、杂环的环,也可以选择性地被氧原子、硫原子或亚胺基所打断,R.sup.3、R.sup.4、R.sup.5和R.sup.6表示氢或较低的烷基,R.sup.5另外表示较低的烷氧基,R.sup.7表示氢、环烷基、苯基或取代苯基、萘基、四氢萘基、噻吩基、呋喃基或吡啶基,A表示化学键或具有多达17个碳原子的烷基、烯基或炔基,以及制备它们的方法、含有这些化合物的药物组合物以及这些药物组合物的用途,这些药物组合物介入胆固醇生物合成。抗高胆固醇物质可用于动脉粥样硬化的治疗和预防;它们抑制酶2,3-环氧齿皮烯-鲍鲁酮合酶。
    公开号:
    US05726205A1
  • 作为产物:
    描述:
    ethyl 4-amino-3-chlorophenylacetate 、 sodium hydroxide 、 溶剂黄146 作用下, 以 四氢呋喃 为溶剂, 反应 14.0h, 以86%的产率得到(4-amino-3-chlorophenyl)acetic acid
    参考文献:
    名称:
    Halogenation of 4-hydroxy/amino-3-methoxyphenyl acetamide TRPV1 agonists showed enhanced antagonism to capsaicin
    摘要:
    As an extension of our analysis of the effect of halogenation on thiourea TRPV1 agonists, we have now modified selected 4-hydroxy(or 4-amino)-3-methoxyphenyl acetamide TRPV1 agonists by 5- or 6-halogenation on the aromatic A-region and evaluated them for potency for TRPV1 binding and regulation and for their pattern of agonism/antagonism (efficacy). Halogenation shifted the functional activity at TRPV1 toward antagonism with a greater extent of antagonism as the size of the halogen increased (I > Br > Cl), as previously observed for the thiourea series. The extent of antagonism was greater for halogenation at the 5-position than at the 6-position, in contrast to SAR for the thiourea series. In this series, compounds 55 and 75 showed the most potent antagonism, with K-i (ant) = 2.77 and 2.19 nM, respectively, on rTRPV1 expressed in Chinese hamster ovary cells. The compounds were thus ca. 40-60-fold more potent than 6'-iodononivamide. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.09.001
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文献信息

  • [EN] 2-PHENYL BENZOYLAMIDES<br/>[FR] 2-PHÉNYLBENZOYLAMIDES
    申请人:PFIZER
    公开号:WO2011145022A1
    公开(公告)日:2011-11-24
    Compounds of Formula I that inhibit microsomal triglyceride transfer protein (MTP) and/or apolipoprotein B (Apo B) secretion and their uses in the treatment of diseases linked thereto in animals are described herein.
    公式I的化合物能够抑制微粒体甘油三酯转运蛋白(MTP)和/或载脂蛋白B(Apo B)的分泌,以及它们在治疗与这些疾病相关的动物疾病中的应用,在本文件中有所描述。
  • [EN] NOVEL EP4 RECEPTOR AGONIST COMPOUNDS<br/>[FR] NOUVEAUX COMPOSÉS AGONISTES DES RÉCEPTEURS EP4
    申请人:GLAXO GROUP LTD
    公开号:WO2009147165A1
    公开(公告)日:2009-12-10
    A compound selected from the group consisting of: (3-chloro-4-[(5-chloro-2-[(2- chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}phenyl)acetic acid; 4-[(5-chloro-2-[(phenylmethyl)oxy]phenyl}carbonyl)amino]phenyl}acetic acid; 3-chloro-4-[(5-chloro-2-[(phenylmethyl)oxy]phenyl}carbonyl)amino]phenyl}acetic acid; (3-chloro-4-[(5-chloro-2-[(3- chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}phenyl)acetic acid; 4-[(2-[(phenylmethyl)oxy]phenyl}carbonyl)amino]phenyl}acetic acid; (4-[(5-chloro-2-[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}-2- fluorophenyl)acetic acid; 3-chloro-4-[(2-[(phenylmethyl)oxy]phenyl}carbonyl)amino]phenyl}acetic acid; (3-chloro-4-[(2-[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}phenyl)acetic acid; 4-[(2-chloro-6-[(phenylmethyl)oxy]phenyl}carbonyl)amino]phenyl}acetic acid; (4-[(2-chloro-6-[(3-chlorophenyl)methyl]oxy}phenyl)carbonyl]amino}phenyl)acetic acid; 4-[(5-chloro-2-[(phenylmethyl)amino]phenyl}carbonyl)amino]phenyl}acetic acid; (4-[(5-chloro-2-[(3-chlorophenyl)methyl]amino}phenyl)carbonyl]amino}phenyl)acetic acid; and (4-[(5-chloro-2-[(2-chlorophenyl)methyl]amino}phenyl)carbonyl]amino}phenyl)acetic acid, or pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising such compounds and the use of such compounds in medicine.
    从以下组中选择的化合物:(3-氯-4-[(5-氯-2-[(2-氯苯基)甲氧基}苯基)羰基]氨基}苯基)乙酸;4-[(5-氯-2-[(苯甲基)氧基]苯基}羰基)氨基]苯基}乙酸;3-氯-4-[(5-氯-2-[(苯甲基)氧基]苯基}羰基)氨基]苯基}乙酸;(3-氯-4-[(5-氯-2-[(3-氯苯基)甲氧基}苯基)羰基]氨基}苯基)乙酸;4-[(2-[(苯甲基)氧基]苯基}羰基)氨基]苯基}乙酸;(4-[(5-氯-2-[(3-氯苯基)甲氧基}苯基)羰基]氨基}-2-氟苯基)乙酸;3-氯-4-[(2-[(苯甲基)氧基]苯基}羰基)氨基]苯基}乙酸;(3-氯-4-[(2-[(3-氯苯基)甲氧基}苯基)羰基]氨基}苯基)乙酸;4-[(2-氯-6-[(苯甲基)氧基]苯基}羰基)氨基]苯基}乙酸;(4-[(2-氯-6-[(3-氯苯基)甲氧基}苯基)羰基]氨基}苯基)乙酸;4-[(5-氯-2-[(苯甲基)氨基]苯基}羰基)氨基]苯基}乙酸;(4-[(5-氯-2-[(3-氯苯基)甲氨基}苯基)羰基]氨基}苯基)乙酸;和(4-[(5-氯-2-[(2-氯苯基)甲氨基}苯基)羰基]氨基}苯基)乙酸,或其药学上可接受的盐,包含这些化合物的药物组合物以及这些化合物在医学上的用途。
  • [EN] INSECTICIDAL DIAZOLE AND TRIAZOLE DERIVATIVES<br/>[FR] DERIVES DE DIAZOLE ET DE TRIAZOLE INSECTICIDES
    申请人:FMC CORP
    公开号:WO2005108374A1
    公开(公告)日:2005-11-17
    It has now been found that certain novel diazole and triazole derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I). Preferred are those compounds of formula (I) where M and Q are carbon; R is methyl; R1 and R2 taken together are -CH=CHCH=CH-, -C(Cl)=CHCH=CH-, -C(F)=CHCH=CH-, or -C(CH3)=CHCH=CH-; X is straight or branched chain alkylenyl; Y is phenyl; and R4 is one or more hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, cyano, amino, or -(O)t-(CH2)v-Z-R6, where Z is -C(R7)=C(R8)-, -C≡C-, or -C(R7)=NO-; and, R6, R7 and R8 are indepdently hydrogen, halogen, or alky. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to the locus of crops where insects are present or are expected to be present.
    已经发现了某些新型二唑和三唑衍生物具有意想不到的杀虫活性。这些化合物由式(I)表示。首选的是式(I)中M和Q为碳;R为甲基;R1和R2一起取-CH=CHCH=CH-, -C(Cl)=CHCH=CH-, -C(F)=CHCH=CH-或-C(CH3)=CHCH=CH-;X为直链或支链烷基;Y为苯基;R4为一个或多个氢、卤素、烷基、卤代烷基、烷氧基、卤代烷氧基、氰基、氨基或-(O)t-(CH2)v-Z-R6,其中Z为-C(R7)=C(R8)-,-C≡C-或-C(R7)=NO-;而R6、R7和R8独立地为氢、卤素或烷基。此外,还公开了包含至少一种式(I)化合物的杀虫有效量和可选地至少一种第二化合物的有效量,以及至少一种杀虫载体的组合物;以及涉及将这些组合物施用于存在或预计存在昆虫的作物生长地点以控制昆虫的方法。
  • THIAZOLYL-DIHYDRO-INDAZOLE
    申请人:GRAUERT Matthias
    公开号:US20070238718A1
    公开(公告)日:2007-10-11
    The present invention relates to new thiazolyl-dihydro-indazoles of general formula (I) wherein the groups R 1 , R 2 and R 3 have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers and the mixtures thereof, and optionally the pharmacologically acceptable acid addition salts, solvates and hydrates thereof, and processes for preparing these thiazolyl-dihydro-indazoles and the use thereof as pharmaceutical compositions.
    本发明涉及一般式(I)的新噻唑基-二氢吲唑,其中基团R1、R2和R3具有权利要求和说明书中给出的含义,其互变体、拉克酸盐、对映体、非对映体和它们的混合物,以及可选择的药理学可接受的酸盐、溶剂合物和水合物,以及制备这些噻唑基-二氢吲唑的方法以及将其用作药物组合物的用途。
  • Gas Barrier Laminated Film and Process for Producing the Same
    申请人:Fujii Hitoshi
    公开号:US20070269664A1
    公开(公告)日:2007-11-22
    There are provided a gas barrier laminated film, which is transparent while possessing excellent gas barrier properties and, at the same time, has excellent impact resistance, and a process for producing the same. The gas barrier laminated film comprises a base material, a vapor deposited film of an inorganic oxide provided on the base material, and a gas barrier coating film provided on the vapor deposited film. The gas barrier laminated film is characterized in that the base material on its side where the vapor deposited film is provided, has been subjected to pretreatment or primer coating treatment, and the gas barrier coating film has been formed by coating a gas barrier coating liquid onto the inorganic oxide film and then heating the coating.
    提供了一种气体阻隔层压膜,它在具有优异气体阻隔性能的同时,具有优异的抗冲击性,且透明。同时提供了制备该压膜的方法。该气体阻隔层压膜包括基材、沉积在基材上的无机氧化物蒸发膜和涂覆在蒸发膜上的气体阻隔涂层膜。该气体阻隔层压膜的特点在于,在蒸发膜所在的基材侧经过预处理或底漆涂层处理,并且气体阻隔涂层膜是通过将气体阻隔涂层液体涂覆在无机氧化物膜上并加热涂覆形成的。
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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