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

1-呋喃-3-乙胺 | 252372-09-1

中文名称
1-呋喃-3-乙胺
中文别名
1-(呋喃-3-基)乙胺
英文名称
1-(3-furyl)ethylamine
英文别名
1-(Furan-3-yl)ethanamine
1-呋喃-3-乙胺化学式
CAS
252372-09-1
化学式
C6H9NO
mdl
MFCD06738794
分子量
111.144
InChiKey
SBVKKZRVKMOURL-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):
    0.2
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    39.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2932190090

反应信息

  • 作为产物:
    描述:
    3-acetylfuran oxime 在 aluminium hydride 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 以62%的产率得到1-呋喃-3-乙胺
    参考文献:
    名称:
    Synthesis of 3-substituted furylethylamines
    摘要:
    DOI:
    10.1007/bf02251702
点击查看最新优质反应信息

文献信息

  • [EN] CYCLOOXYGENASE-2 INHIBITORS AND USES THEREOF<br/>[FR] INHIBITEURS DE CYCLO-OXYGÉNASE 2 ET LEURS UTILISATIONS
    申请人:BROAD INST INC
    公开号:WO2021050700A1
    公开(公告)日:2021-03-18
    The present disclosure describes compounds of the formula: (I), (II), (III), (IV), (V). The compounds described herein may be cyclooxygenase (COX) (e.g., cyclooxygenase 2 (COX2)) inhibitors. The compounds may be radiolabeled. The compounds (e.g., radiolabeled compounds) may be useful (e.g., as positron emission tomography (PET) imaging agents) for diagnosing a disease. The compounds may also be useful for treating or preventing a disease. The present disclosure also describes pharmaceutical compositions and kits including the compounds; and methods of using the compounds.
    本公开描述了以下式的化合物:(I),(II),(III),(IV),(V)。本文描述的化合物可能是环氧合酶(COX)(例如,环氧合酶2(COX2))抑制剂。这些化合物可能被放射标记。这些化合物(例如,放射标记化合物)可能用于诊断疾病(例如,作为正电子发射断层扫描(PET)成像剂)。这些化合物也可能用于治疗或预防疾病。本公开还描述了包括这些化合物的药物组合物和试剂盒;以及使用这些化合物的方法。
  • 3-(4-AMINOPHENYL)-2-FURANCARBOXYLIC ACID DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF
    申请人:Fujii Akihito
    公开号:US20120059012A1
    公开(公告)日:2012-03-08
    Disclosed is a compound represented by Formula (I) or a pharmaceutically acceptable salt thereof: wherein R 1 is 1: a C 3-8 cycloalkyl C 1-4 alkyl group, 2: a C 7-14 aralkyl group, in which the aryl moiety thereof is optionally substituted with the same or different 1 to 3 groups selected from the group consisting of: (a) halogen, (b) C 1-4 alkyl, which is optionally substituted with 1 to 3 fluorine atoms, (c) C 1-4 alkoxy, which is optionally substituted with 1 to 3 fluorine atoms, and (d) C 1-4 alkylcarbonyl, which is optionally substituted with C 1-4 alkoxy, 3: a five- to ten-membered heteroaryl-C 1-4 alkyl group, in which the heteroaryl moiety thereof is optionally substituted with the same or different 1 to 3 groups selected from the group consisting of: (a) halogen, and (b) C 1-4 alkyl, or 4: a C 6-10 aryl C 2-6 alkenyl group; and R 2 is a cyano group or a nitro group.
    揭示了由化学式(I)表示的化合物或其药学上可接受的盐:其中R1是1:C3-8环烷基C1-4烷基基团,2:C7-14芳基烷基基团,其中其芳基部分可选择性地取代为来自以下组成的1至3个相同或不同的基团:(a)卤素,(b)C1-4烷基,可选择性地取代为1至3个原子,(c)C1-4烷氧基,可选择性地取代为1至3个原子,和(d)C1-4烷基羰基,可选择性地取代为C1-4烷氧基,3:五元至十元杂芳基-C1-4烷基基团,其中其杂芳基部分可选择性地取代为来自以下组成的1至3个相同或不同的基团:(a)卤素,和(b)C1-4烷基,或4:C6-10芳基C2-6烯基基团;和R2是基或硝基基团。
  • Novel aminotransferase, gene encoding the same, and method of using them
    申请人:Ito Noriyuki
    公开号:US20100285544A1
    公开(公告)日:2010-11-11
    The invention relates to a novel aminotransferase, DNA encoding the enzyme, a recombinant vector into which the DNA has been introduced, and a transformant into which the vector has been introduced. Further, the invention also relates to a method for producing an optically active amino compound utilizing the enzyme or transformant. The aminotransferase of the invention has an ability of efficiently converting a ketone compound, particularly a cyclic ketone compound to an optically active amino compound. According to the invention, a method for efficiently producing an optically active amino compound, particularly an optically active cyclic amino compound is provided.
    本发明涉及一种新型基转移酶、编码该酶的DNA、已引入该DNA的重组载体以及已引入该载体的转化菌株。此外,本发明还涉及一种利用该酶或转化菌株生产光学活性氨基化合物的方法。本发明的基转移酶能够高效地将酮类化合物,尤其是环状酮类化合物转化为光学活性氨基化合物。根据本发明,提供了一种高效生产光学活性氨基化合物,尤其是光学活性环状氨基化合物的方法。
  • NOVEL AMINOTRANSFERASE, GENE ENCODING THE SAME, AND METHODS OF USING THEM
    申请人:ITO NORIYUKI
    公开号:US20120164724A1
    公开(公告)日:2012-06-28
    The invention relates to a novel aminotransferase, DNA encoding the enzyme, a recombinant vector into which the DNA has been introduced, and a transformant into which the vector has been introduced. Further, the invention also relates to a method for producing an optically active amino compound utilizing the enzyme or transformant. The aminotransferase of the invention has an ability of efficiently converting a ketone compound, particularly a cyclic ketone compound to an optically active amino compound. According to the invention, a method for efficiently producing an optically active amino compound, particularly an optically active cyclic amino compound is provided.
    本发明涉及一种新型基转移酶、编码该酶的DNA、将该DNA引入的重组载体以及将该载体引入的转化体。此外,本发明还涉及利用该酶或转化体生产光学活性氨基化合物的方法。本发明中的基转移酶能够有效地将酮化合物,特别是环状酮化合物转化为光学活性氨基化合物。根据本发明,提供了一种有效生产光学活性氨基化合物,特别是光学活性环状氨基化合物的方法。
  • (S)-alpha-PHENETHYLAMINE : PYRUVATE TRANSAMINASE
    申请人:KANEKA CORPORATION
    公开号:EP1045025A1
    公开(公告)日:2000-10-18
    Relating to an enzyme capable of efficiently converting a ketone compound to an optically active amino compound by transamination, and a process for preparing an optically active amino compound using the enzyme. An (S)-α-phenethylamine : pyruvate transaminase, which acts on (S)-α-phenethylamine and a ketone compound, thereby catalyzing transamination for forming acetophenone and an amino compound corresponding to the ketone compound; a process for preparing an optically active amino compound using the transaminase; and a method for culturing a microorganism for producing the above transaminase, comprising adding to a medium one or more compounds selected from the group consisting of propylamine, 1-butylamine, 2-butylamine, 2-pentylamine, isopropylamine and isobutylamine as an inducer for the enzyme when a microorganism for producing (S)-α-phenethylamine : pyruvate transaminase is cultured.
    涉及一种能够通过转基作用将酮化合物有效转化为光学活性氨基化合物的酶,以及使用该酶制备光学活性氨基化合物的工艺。一种(S)-α-苯乙胺丙酮酸酶,它作用于(S)-α-苯乙胺和酮化合物,从而催化转作用以形成苯乙酮和与酮化合物相对应的氨基化合物;使用该转酶制备光学活性氨基化合物的工艺;和一种培养产生上述转酶的微生物的方法,包括当产生(S)-α-苯乙胺的微生物时,在培养基中加入一种或多种选自由丙胺1-丁胺2-丁胺2-戊胺异丙胺异丁胺组成的组的化合物作为酶的诱导剂:丙酮酸酶的微生物
查看更多

同类化合物

(乙腈)二氯镍(II) (R)-(-)-α-甲基组胺二氢溴化物 (N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-3-氨基环丁烷甲腈盐酸盐 顺式-2-羟基甲基-1-甲基-1-环己胺 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺二盐酸盐 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷