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N-(9H-芴-2-基)苯甲酰胺 | 3671-78-1

中文名称
N-(9H-芴-2-基)苯甲酰胺
中文别名
——
英文名称
N-2-fluorenylbenzamide
英文别名
2-Benzoylaminofluorene;N-(9H-fluoren-2-yl)benzamide
N-(9H-芴-2-基)苯甲酰胺化学式
CAS
3671-78-1
化学式
C20H15NO
mdl
——
分子量
285.345
InChiKey
MEZOSXXWXWNPDU-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:
    215 °C
  • 沸点:
    427.77°C (rough estimate)
  • 密度:
    1.1281 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    5.3
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2924299090

SDS

SDS:9ecc198490fad2c4b5a2d77156478761
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

反应信息

  • 作为反应物:
    描述:
    N-(9H-芴-2-基)苯甲酰胺sodium methylate碳酸氢钠 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 2.5h, 生成 N-(4a-hydroxy-9a-methoxy-9H-fluoren-2-yl)benzamide
    参考文献:
    名称:
    Preparation of quinol N-acyl- and quinol ether imines via anodic oxidation of para-substituted anilide derivatives
    摘要:
    Anodic oxidation of N-benzoyl-4-methylaniline in 5 % aqueous methanol in the presence of sodium bicarbonate affords two major products: 4-methoxy-4-methylbenzoquinol N-benzoylimine, 8a, and a dimer, 4-[N-benzoyl-N-(4-methylphenyl)amino]-4-methylbenzoquinol N-benzoylimine, 9. The ratio of these two products was temperature dependent, and conditions were developed for preparing 8a and 9 in good yield. Using the conditions developed for 8a, the anodic methoxylation of N-benzoyl and acetyl derivatives of 4-ethyl- and 4-sec-butyl-4-phenylaniline and 2-aminofluorene derivatives was performed. The yields of the N-benzoyl derivatives of the 4-methoxy-4-substituted-benzoquinol imines were 46-80%, while the N-acetyl derivatives gave lower yields. When the anodic oxidation was performed using 30% water/acetonitrile or 10 % water/tetrahydrofuran, the 4-alkylbenzoquinol N-benzoylimine derivatives were obtained. The yields of these anodic hydroxylation reactions were lower than those of the corresponding methoxylations for all systems studied. In addition, the 4-alkylbenzoquinol N-benzoylimine derivatives were much more labile. Two methods were developed for conversion of the 4-methoxy-4-substituted-benzoquinol N-acylimines to the 4-methoxy-4-substituted-benzoquinol N-alkylimines. Finally, the especially labile 4-hydroxy-4-phenylbenzoquinol N-acetylimine was prepared for the first time from the readily available N-benzoyl derivative.
    DOI:
    10.1021/jo00073a016
  • 作为产物:
    描述:
    2-氨基芴 以80%的产率得到
    参考文献:
    名称:
    FARCASAN, V.;PAIU, F.;OLTEANU, I.;DEMIAN, H., STUD. UNIV. BABES-BOLYAI. CHEM., 1985, 30, 5-10
    摘要:
    DOI:
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文献信息

  • Chromium-Catalyzed Activation of Acyl C–O Bonds with Magnesium for Amidation of Esters with Nitroarenes
    作者:Liang Ling、Changpeng Chen、Meiming Luo、Xiaoming Zeng
    DOI:10.1021/acs.orglett.9b00554
    日期:2019.3.15
    chromium-catalyzed activation of acyl C–O bonds with magnesium for amidation of esters with nitroarenes. Low-cost chromium(III) chloride shows high reactivity in promoting amidation by using magnesium as reductant and chlorotrimethylsilane as additive. It provides a step-economic strategy to the synthesis of centrally important amide motifs using inexpensive and air-stable nitroarenes as amino sources.
    在这里,我们报道了铬与镁催化的羰基C–O键活化,从而使酯与硝基芳烃酰胺化。通过使用镁作为还原剂和氯代三甲基硅烷作为添加剂,低成本的氯化铬(III)在促进酰胺化方面显示出高反应活性。它为使用廉价且空气稳定的硝基芳烃作为氨基源合成重要的酰胺基序提供了分步经济策略。
  • [EN] BAX AGONIST, COMPOSITIONS, AND METHODS RELATED THERETO<br/>[FR] AGONISTE DE BAX, COMPOSITIONS ET PROCÉDÉS ASSOCIÉS
    申请人:UNIV EMORY
    公开号:WO2013028543A1
    公开(公告)日:2013-02-28
    The disclosure relates to BAX activators and therapeutic uses relates thereto. In certain embodiments, the disclosure relates to methods of treating or preventing cancer, such as lung cancer, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a compound disclosed herein or pharmaceutically acceptable salt to a subject in need thereof.
    本公开涉及BAX激活剂及其治疗用途。在某些实施例中,本公开涉及治疗或预防癌症的方法,例如肺癌,包括向需要的受试者施用本公开的化合物或药学上可接受的盐所述的药物组合的治疗有效量。
  • COMPOSITIONS AND METHODS FOR TREATMENT OF VIRAL DISEASES
    申请人:Johansen Lisa M.
    公开号:US20100009970A1
    公开(公告)日:2010-01-14
    The present invention features compositions, methods, and kits useful in the treatment of viral diseases. In certain embodiments, the viral disease is caused by a single stranded RNA virus, a flaviviridae virus, or a hepatic virus. In particular embodiments, the viral disease is viral hepatitis (e.g., hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E) and the agent or combination of agents includes sertraline, a sertraline analog, UK-416244, or a UK-416244 analog. Also featured are screening methods for identification of novel compounds that may be used to treat a viral disease.
    本发明涉及用于治疗病毒性疾病的组合物、方法和试剂盒。在某些实施方式中,病毒性疾病是由单链RNA病毒、黄病毒科病毒或肝病毒引起的。在特定实施方式中,病毒性疾病是病毒性肝炎(例如甲型肝炎、乙型肝炎、丙型肝炎、丁型肝炎、戊型肝炎),药剂或药剂组合包括舍曲林、舍曲林类似物、UK-416244或UK-416244类似物。还包括用于鉴定可用于治疗病毒性疾病的新化合物的筛选方法。
  • BAX AGONIST, COMPOSITIONS, AND METHODS RELATED THERETO
    申请人:Deng Xingming
    公开号:US20140178374A1
    公开(公告)日:2014-06-26
    The disclosure relates to BAX activators and therapeutic uses relates thereto. In certain embodiments, the disclosure relates to methods of treating or preventing cancer, such as lung cancer, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a compound disclosed herein or pharmaceutically acceptable salt to a subject in need thereof.
    该披露涉及BAX活化剂及其治疗用途。在某些实施例中,该披露涉及治疗或预防癌症的方法,例如肺癌,包括向需要该治疗的受试者施用含有此处披露的化合物或药学上可接受的盐的药物组合物的治疗有效量。
  • THE RELATIVE PROPORTIONS OF STEREOISOMERIC OXIMES FORMED IN THE OXIMATION OF UNSYMMETRICAL KETONES
    作者:W. E. BACHMANN、SISTER M. XAVERIA BARTON
    DOI:10.1021/jo01221a003
    日期:1938.9
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