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4-甲氧基苯并呋喃 | 18014-96-5

中文名称
4-甲氧基苯并呋喃
中文别名
——
英文名称
4-methoxybenzofuran
英文别名
4-methoxy-1-benzofuran
4-甲氧基苯并呋喃化学式
CAS
18014-96-5
化学式
C9H8O2
mdl
——
分子量
148.161
InChiKey
NWCMFNIMUUMBGZ-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:
    220-222 °C
  • 密度:
    1.136±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    22.4
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    4-甲氧基苯并呋喃双三甲基硅氧基甲基硅烷3,3-二甲基-1-丁烯 、 C25H40O2P2Ru 作用下, 以 neat (no solvent) 为溶剂, 反应 6.0h, 以94%的产率得到3-(4-methoxybenzofuran-2-yl)-1,1,1,3,5,5,5-heptamethyltrisiloxane
    参考文献:
    名称:
    A Pincer Ruthenium Complex for Regioselective C–H Silylation of Heteroarenes
    摘要:
    A pincer Ru(II) catalyst for the highly efficient undirected silylation of O- and S-heteroarenes with (TMSO)(2)MeSiH and Et3SiH is described, producing heteroarylsilanes with exclusive C2-regioselectivity, good functional group tolerance, and high turnover numbers (up to 1960). The synthetic utility of the silylated products is demonstrated by Pd-catalyzed Hiyama-Denmark cross-coupling under mild conditions. One-pot, two-step silylation and coupling procedures have been also developed.
    DOI:
    10.1021/acs.orglett.6b02857
  • 作为产物:
    描述:
    参考文献:
    名称:
    Limaye, Rasayanam, 1936, vol. 1, p. 1,14
    摘要:
    DOI:
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文献信息

  • Dioxazolones as masked ester surrogates in the Pd(<scp>ii</scp>)-catalyzed direct C–H arylation of 6,5-fused heterocycles
    作者:Paridhi Saxena、Neha Maida、Manmohan Kapur
    DOI:10.1039/c9cc05563k
    日期:——
    simple and effective Pd(II)-catalyzed regioselective C(2)–H arylation of 6,5-fused heterocycles with dioxazolones as a masked ester surrogate under mild conditions is reported. The significance of the arylation is highlighted by the new reactivity demonstrated in dioxazolones via proximal C–H activation of the cyclic carbonate of the hydroxamic acid functionality under protic conditions.
    据报道,在温和的条件下,一种简单有效的Pd(II)催化6,5-稠合杂环与二恶唑酮作为掩蔽酯替代物的区域选择性C(2)–H芳基化反应。通过在质子条件下通过近端C–H活化异羟肟酸官能团的环状碳酸酯在二恶唑酮中显示出新的反应性,突出了芳基化的重要性。
  • ANTI-HIV COMPOUNDS
    申请人:Prosetta Antiviral, Inc.
    公开号:US20160168100A1
    公开(公告)日:2016-06-16
    This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
    这项发明提供了用于治疗病毒感染的四氢异喹啉等化合物,含有这类化合物的药物配方,以及抑制病毒(如HIV)复制或治疗疾病(如艾滋病)的方法。
  • Phenoxypropylamine compounds
    申请人:——
    公开号:US20020111358A1
    公开(公告)日:2002-08-15
    The present invention relates to a phenoxypropylamine compound of the formula (I) 1 wherein each symbol is as defined in the specification, an optically active compound thereof or a pharmaceutically acceptable salt thereof and hydrates thereof, which simultaneously show selective affinity for and antagonistic activity against 5-HT 1A receptor, as well as 5-HT reuptake inhibitory activity, and can be used as antidepressants quick in expressing an anti-depressive effect.
    本发明涉及一种公式(I)中的苯氧丙胺化合物: 1 其中每个符号如说明书中所定义,其光学活性化合物或其药物可接受的盐及水合物,同时显示出对5-HT 1A 受体的选择性亲和力和拮抗活性,以及5-HT再摄取抑制活性,并且可以用作快速表达抗抑郁效果的抗抑郁药。
  • [EN] 6-HYDROXYBENZOFURANYL- AND 6-ALKOXYBENZOFURANYL-SUBSTITUTED IMIDAZOPYRIDAZINES<br/>[FR] IMIDAZOPYRIDAZINES 6-HYDROXYBENZOFURANYL- ET 6-ALCOXYBENZOFURANYL-SUBSTITUÉES
    申请人:BAYER PHARMA AG
    公开号:WO2016102427A1
    公开(公告)日:2016-06-30
    The present invention relates to 6-hydroxybenzofuranyl- and 6-alkoxybenzofuranyl- substituted imidazopyridazine compounds of general formula (I) in which R1 and R2 are as defined in the claims, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients.
    本发明涉及一般式(I)中R1和R2如权利要求中所定义的6-羟基苯并呋喃基和6-烷氧基苯并呋喃基取代的咪唑吡啶嗪化合物,以及制备所述化合物的方法,用于制备所述化合物的有用中间体化合物,包含所述化合物的药物组合物和组合物,以及利用所述化合物制造用于治疗或预防疾病的药物组合物,特别是用作唯一药剂或与其他活性成分组合使用,用于治疗或预防过度增殖和/或血管生成紊乱的疾病。
  • POLYMERIZABLE MONOMER, POLYMER COMPOUND FOR CONDUCTIVE POLYMER, AND METHOD FOR PRODUCING THE POLYMER COMPOUND
    申请人:SHIN-ETSU CHEMICAL CO., LTD.
    公开号:US20200247926A1
    公开(公告)日:2020-08-06
    Polymerization reaction is performed using a polymerizable monomer shown by the following general formula (1) and at least one monomer selected from monomers each having a structure of a salt among a lithium salt, a sodium salt, a potassium salt, and a nitrogen compound salt of a fluorosulfonic acid or the like; then, the structure of the salt of the repeating unit of a polymer obtained by the polymerization reaction is changed to the fluorosulfonic acid or the like by ion exchange. Thus, the present invention provides a polymer compound for a conductive polymer and a method for producing the polymer compound which is suitably used as a dopant for a fuel cell and a conductive material, and which is a copolymer containing a repeating unit of styrene having a 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylisobutyl ether group, and a repeating unit having any of a fluorosulfonic acid, a fluorosulfonimide group, and a n-carbonyl-fluoro-sulfonamide group.
    聚合反应使用以下一般式(1)所示的可聚合单体和至少一种选择自锂盐、钠盐、钾盐和氟磺酸盐等盐结构的单体中的单体进行;然后,通过离子交换将聚合反应得到的聚合物的重复单元的盐结构改变为氟磺酸盐或类似物。因此,本发明提供了一种用作导电聚合物的聚合物化合物以及用作燃料电池和导电材料的掺杂剂的聚合物化合物的生产方法,该聚合物是含有3,3,3-三氟-2-羟基-2-三氟甲基异丁基醚基的苯乙烯重复单元和具有氟磺酸、氟磺酰亚胺基团和n-羰基-氟磺酰胺基团中的任何一种的重复单元的共聚物。
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同类化合物

顺式-1-((2-(5-氯-2-苯并呋喃基)-4-甲基-1,3-二氧戊环-2-基)甲基)-1H-1,2,4-三唑 顺式-1-((2-(5,7-二氯-2-苯并呋喃基)-4-乙基-1,3-二氧戊环-2-基)甲基)-1H-咪唑 顺式-1-((2-(2-苯并呋喃基)-4-乙基-1,3-二氧戊环-2-基)甲基)-1H-1,2,4-三唑 霉酚酸酯杂质B 间甲酚紫 间甲基苯基(苯并呋喃-2-基)甲醇 长管假茉莉素C 金霉素 酪氨酸,b-羰基- 酞酸酐-d4 酚酞二丁酸酯 酚酞 酚红钠 酚红 邻苯二甲酸酐与马来酸酐,甘氨酰蜡素和二乙二醇的聚合物 邻苯二甲酸酐与己二醇的聚合物 邻苯二甲酸酐与三甘醇异壬醇的聚合物 邻苯二甲酸酐与2-乙基-2-羟甲基-1,3-丙二醇和2,5-呋喃二酮的聚合物 邻苯二甲酸酐与2-乙基-2-羟甲基-1,3-丙二醇、2,5-呋喃二酮和2-乙基己酸苯甲酸酯的聚合物 邻苯二甲酸酐-4-硼酸频哪醇酯 邻苯二甲酸酐,马来酸,二乙二醇,新戊二醇聚合物 邻甲酚酞 贝康唑 表灰黄霉素 螺佐呋酮 螺[苯并呋喃-3(2H),4-哌啶] 螺[异苯并呋喃-1(3H),4’-哌啶]-3-酮 螺[异苯并呋喃-1(3H),4'-哌啶]-3-酮盐酸盐 螺[异苯并呋喃-1(3H),3’-吡咯烷]-3-酮 螺[1-苯并呋喃-2,1'-环丙烷]-3-酮 薄荷内酯 莫罗卡尼 荨麻叶泽兰酮 荧光胺 苯酞-3-乙酸 苯酐二乙二醇共聚物 苯酐 苯甲酸,2-[(1,3-二羰基丁基)氨基]-,甲基酯 苯甲酸,2,2-二(羟甲基)丙烷-1,3-二醇,异苯并呋喃-1,3-二酮 苯甲酰氯化,3-甲氧基-4-甲基- 苯甲基(1-{(2-amino-2-methylpropanoyl)[(2S)-2-aminopropanoyl]amino}-2-methyl-1-oxopropan-2-yl)甲基氨基甲酸酯(non-preferredname) 苯并呋喃并[3,2-d]嘧啶-2,4(1H,3H)-二酮 苯并呋喃并[3,2-D]嘧啶-4(1H)-酮 苯并呋喃并[2,3-d]哒嗪-4(3H)-酮 苯并呋喃并(3,2-c)吡啶,1,2,3,4-四氢-2-(2-(二甲氨基)乙基)-,二盐酸 苯并呋喃与1H-茚的聚合物 苯并呋喃[3,2-b]吡咯-2-羧酸 苯并呋喃-7-羧酸 苯并呋喃-7-硼酸频那醇酯 苯并呋喃-7-甲腈