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2-甲氧基-4-苯基氨基甲基-苯酚 | 58285-77-1

中文名称
2-甲氧基-4-苯基氨基甲基-苯酚
中文别名
——
英文名称
4-anilinomethyl-2-methoxyphenol
英文别名
4-(Anilinomethyl)-2-methoxy-phenol;4-(anilinomethyl)-2-methoxyphenol
2-甲氧基-4-苯基氨基甲基-苯酚化学式
CAS
58285-77-1
化学式
C14H15NO2
mdl
——
分子量
229.279
InChiKey
UKQLNPDOROJMTD-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

  • 熔点:
    250 °C(Solv: methanol (67-56-1))
  • 沸点:
    398.6±27.0 °C(Predicted)
  • 密度:
    1.193±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    41.5
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:0fb59547abeb8f9f59b3ef2fcd265716
查看

上下游信息

  • 下游产品
    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:
    2-甲氧基-4-苯基氨基甲基-苯酚硫代异氰酸苯酯氯仿 为溶剂, 以71%的产率得到1-(4-Hydroxy-3-methoxybenzyl)-1, 3-diphenylthiourea (1b)
    参考文献:
    名称:
    Synthesis and biological evaluation of novel N, N′-disubstituted urea and thiourea derivatives as potential anti-melanoma agents
    摘要:
    Two series of urea and thiourea derivatives (1a-11a, 1b-11b) have been synthesized; all the 22 compounds were reported for the first time. Their anti-proliferative activities against the melanoma cell line B16-F10 were evaluated. Among the compounds tested, compound 6b exhibited the most potent activity in melanoma cells growth inhibition (IC50 = 0.33 mu M). The bioassay tests showed that anti-proliferative activities of these novel compounds were possibly caused by inhibition of ERK1/2 phosphorylation level. Therefore, compound 6b can be a potential anti-melanoma agent and an inhibitor of ERK1/2 phosphorylation deserving further research.
    DOI:
    10.3109/14756366.2011.608665
  • 作为产物:
    描述:
    N-(4-hydroxy-3-methoxybenzylidene)aniline 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 2.0h, 生成 2-甲氧基-4-苯基氨基甲基-苯酚
    参考文献:
    名称:
    Synthesis and biological evaluation of novel N, N′-disubstituted urea and thiourea derivatives as potential anti-melanoma agents
    摘要:
    Two series of urea and thiourea derivatives (1a-11a, 1b-11b) have been synthesized; all the 22 compounds were reported for the first time. Their anti-proliferative activities against the melanoma cell line B16-F10 were evaluated. Among the compounds tested, compound 6b exhibited the most potent activity in melanoma cells growth inhibition (IC50 = 0.33 mu M). The bioassay tests showed that anti-proliferative activities of these novel compounds were possibly caused by inhibition of ERK1/2 phosphorylation level. Therefore, compound 6b can be a potential anti-melanoma agent and an inhibitor of ERK1/2 phosphorylation deserving further research.
    DOI:
    10.3109/14756366.2011.608665
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文献信息

  • Synthesis of an Fe–Pd bimetallic catalyst for <i>N</i>-alkylation of amines with alcohols <i>via</i> a hydrogen auto-transfer methodology
    作者:Peng-yu Wu、Guo-ping Lu、Chun Cai
    DOI:10.1039/d0gc03725g
    日期:——
    systems, and thus the exploration of a highly efficient and recyclable heterogeneous catalyst remains meaningful. In this work, a novel bimetallic catalyst, Fe10Pd1/NC500 derived from bimetallic MOF NH2-MIL-101(Fe10Pd1), has been prepared, and the catalyst exhibits superior catalytic performance for the N-alkylation of amines with alcohols via a hydrogen auto-transfer methodology. High yields of the
    从经济和环境的角度来看,结合脱氢,中间反应和氢化的氢自动转移(HAT)或借用氢(BH)方法被认为是一锅合成的绝佳策略。尽管已经为开发用于HAT反应的催化剂做出了很多努力,但是在大多数报道的催化系统中仍然需要苛刻的条件,外部碱或大量的贵金属,因此,探索一种高效且可回收的多相催化剂仍然有意义。在这项工作中,一种新型的双金属催化剂Fe 10 Pd 1 / NC500衍生自双金属MOF NH 2 -MIL-101(Fe 10 Pd 1),并且通过氢自动转移方法,该催化剂对胺与醇的N-烷基化表现出优异的催化性能。在120℃下,醇/胺的摩尔比为2∶1,不需要的外部添加剂或溶剂就可以得到高产率的所需产物。与单金属催化剂相比,观察到了催化性能的显着提高,这可以归因于双金属合金内部的“协同效应”。已经揭示出N掺杂的碳载体可提供必要的碱性,从而避免了对外部碱的需求。此外,Fe 10 Pd 1显示了宽的基材范围和出色的可重复使用性/
  • Niobium Oxide Supported on Cubic Spinel Cobalt Oxide as an Efficient Heterogeneous Catalyst for the Synthesis of Imines via Dehydrogenative Coupling of Amines and Alcohols
    作者:Balasaheb D. Bankar、Krishnan Ravi、Saravanan Subramanian、Ankush V. Biradar
    DOI:10.1007/s10562-022-03943-2
    日期:2022.12
    results are confirmed further by PXRD d-spacing. Whereas cobalt oxide exists in (2 2 2), (3 1 1), and (1 1 1) facet, which confirms the crystal cubic spinel structure of Co3O4. The TPD ammonia desorption Nb2O5/Co3O4 result confirms the presence of 0.441 mmol/g acidic sites. The synthesized Nb2O5/Co3O4 catalyst effectively transformed aromatic amines and benzyl alcohols to imines through a dehydrogenative
    开发用于脱氢转化的可持续化学过程为选择性合成含氮化合物带来了可喜的结果。我们报道了使用共沉淀法合成 Nb 2 O 5 /Co 3 O 4催化剂,然后是水热法。FESEM、NH 3 -TPD、PXRD、FT-IR吡啶吸附研究和XPS用于表征合成材料的化学和结构性质。FESEM分析显示Nb均匀地分布在Co 3 O 4的表面上。3.3 wt% Nb 在 Co 3 O 4上显示出 (2 5 0) 和 (0 0 1) 晶面,并且这些结果通过 PXRD d-间距进一步证实。而氧化钴存在于(2 2 2)、(3 1 1)和(1 1 1)晶面,这证实了Co 3 O 4的晶体立方尖晶石结构。TPD 氨解吸 Nb 2 O 5 /Co 3 O 4结果证实存在 0.441 mmol/g 酸性位点。合成的Nb 2 O 5 /Co 3 O 4催化剂通过脱氢偶联反应有效地将芳香胺和苯甲醇转化为亚胺。3.3 wt% Nb 2
  • Redox-Neutral Intramolecular Dearomative Spirocyclization of Phenols Induced by Visible Light
    作者:Linlin Zhang、Fengchi Hu、Lei Shen、Lijuan Gao、Yunhong Yang、Zhiqiang Pan、Chengfeng Xia
    DOI:10.1021/acs.orglett.3c01257
    日期:2023.5.5
    spirocyclohexadienone. Mechanistic experiments revealed that the aryl halide was reduced to aryl radical via the single-electron transfer (SET) process under visible light irradiation. The electrophilic addition of an aryl radical with the phenolate anion moiety gave a radical anion intermediate, which recycled the photocatalyst by a second SET process.
    本文描述的是由可见光诱导的氧化还原中性分子内脱芳环化。光化学环化由酚盐阴离子衍生的光催化剂催化,并产生螺环己二烯酮。机理实验表明,芳基卤化物在可见光照射下通过单电子转移 (SET) 过程还原为芳基自由基。芳基与酚盐阴离子部分的亲电加成产生自由基阴离子中间体,通过第二个 SET 过程回收光催化剂。
  • A reusable MOF supported single-site nickel-catalyzed direct N-alkylation of anilines with alcohols
    作者:Yuanyuan Lu、Huining Chai、Kun Yu、Chaonan Huang、Yujie Li、Jinyu Wang、Jiping Ma、Weiqiang Tan、Guangyao Zhang
    DOI:10.1016/j.tet.2022.132993
    日期:2022.10
    The direct N-alkylation of amines with alcohols is an efficient route through a borrowing hydrogen (BH) strategy. Herein, a highly selective, and reusable Ni(II)-bipyridine-based metal-organic framework (MOF) catalyst was designed for this organic transformation. This earth-abundant metal-based metal-organic framework (MOF) catalyst significantly outperform their homogeneous analogues and the immobilized
    胺与醇的直接N-烷基化是通过借氢 (BH) 策略的有效途径。在此,为这种有机转化设计了一种高选择性、可重复使用的 Ni(II)-联吡啶基金属有机骨架 (MOF) 催化剂。这种富含地球的金属基金属有机骨架 (MOF) 催化剂显着优于其均相类似物,并且固定化催化剂可重复使用至少 4 个循环,而目标产物的产率不会显着降低。
  • Rai, Mangat; Kumar, Surinder; Singh, Baldev, Journal of the Indian Chemical Society, 1982, vol. 59, # 1, p. 80 - 81
    作者:Rai, Mangat、Kumar, Surinder、Singh, Baldev、Krishan, Kewal、Singh, Ajit
    DOI:——
    日期:——
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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