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Ethyl 1-(N-Methylamino)-5,6,7,8-tetrafluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate | 141449-63-0

中文名称
——
中文别名
——
英文名称
Ethyl 1-(N-Methylamino)-5,6,7,8-tetrafluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate
英文别名
ethyl 5,6,7,8-tetrafluoro-1-(methylamino)-4-oxoquinoline-3-carboxylate
Ethyl 1-(N-Methylamino)-5,6,7,8-tetrafluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate化学式
CAS
141449-63-0
化学式
C13H10F4N2O3
mdl
——
分子量
318.228
InChiKey
DMESACZSTFIXKU-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):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    58.6
  • 氢给体数:
    1
  • 氢受体数:
    9

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

点击查看最新优质反应信息

文献信息

  • Certain tricyclic pyrido[3,2,1-ij]cinnoline-8-carboxylates, useful as
    申请人:Wakunaga Pharmaceutical Co., Ltd.
    公开号:US05359066A1
    公开(公告)日:1994-10-25
    A compound represented by the following general formula: ##STR1## which is useful as an intermediate for production of a clinically excellent synthetic antibacterial, a salt thereof, and a process for producing the same. In said formula, R.sup.1 is a hydrogen atom or a carboxyl-protecting group; R.sup.2 is a hydrogen atom or a lower alkyl group; X.sup.1 is a hydrogen atom or a halogen atom; X.sup.2 is a halogen atom; X.sub.a.sup.5 is a hydrogen atom or a halogen atom; A is a methylene group; a group of >CH--COOR.sup.4, etc., in which R.sup.4, R.sup.5 and R.sup.6 each are a hydrogen atom or a carboxyl-protecting group; B is a methylene group or a carbonyl group; provided that both A and B must not be methylene groups at the same time.
    以下是一种化合物的通用公式:##STR1##,它可用作合成临床上优良的合成抗菌剂的中间体,其盐以及制备该化合物的方法。在上述公式中,R.sup.1是氢原子或羧基保护基;R.sup.2是氢原子或较低的烷基基团;X.sup.1是氢原子或卤素原子;X.sup.2是卤素原子;X.sub.a.sup.5是氢原子或卤素原子;A是亚甲基基团;一个>CH--COOR.sup.4等基团,其中R.sup.4、R.sup.5和R.sup.6分别是氢原子或羧基保护基;B是亚甲基基团或羰基基团;但必须同时满足A和B不能都是亚甲基基团。
  • Novel tricyclic compound or salts thereof, method for producing the same and antimicrobial agent containing the same
    申请人:WAKUNAGA SEIYAKU KABUSHIKI KAISHA
    公开号:EP0470578A1
    公开(公告)日:1992-02-12
    A tricyclic compound represented by the general formula (1) and salts thereof. A method for producing the tricyclic compound and salts thereof, and an antimicrobial agent containing the tricyclic compound and salts thereof as an active ingredient are also disclosed.
    由通式(1)代表的三环化合物及其盐类。 此外,还公开了一种生产该三环化合物及其盐类的方法,以及一种含有该三环化合物及其盐类作为活性成分的抗菌剂。
  • PROCESS FOR PRODUCING TRICYCLIC COMPOUND OR SALT THEREOF
    申请人:FUJISAWA PHARMACEUTICAL CO., LTD.
    公开号:EP0530368A1
    公开(公告)日:1993-03-10
    A compound represented by general formula (I), which is useful as an intermediate for the production of a clinically excellent synthetic antibacterial, a salt thereof, and a process for producing the same. In said formula, R¹ represents hydrogen or a carboxyl protective group, R² represents hydrogen or lower alkyl, X¹ represents hydrogen or halogen, X² represents halogen, X⁵a represents hydrogen or halogen, A represents methylene, =CH-COOR⁴, etc., and B represents methylene or carbonyl, provided that A and B should not be methylene groups at the same time.
    一种通式(I)代表的化合物,它可作为生产临床上极好的合成抗菌剂的中间体、其盐及其生产工艺。在所述式中,R¹代表氢或羧基保护基,R²代表氢或低级烷基,X¹代表氢或卤素,X²代表卤素,X⁵a代表氢或卤素,A代表亚甲基、=CH-COOR⁴等,B代表亚甲基或羰基,但A和B不应同时为亚甲基。
  • US5254685A
    申请人:——
    公开号:US5254685A
    公开(公告)日:1993-10-19
  • US5359066A
    申请人:——
    公开号:US5359066A
    公开(公告)日:1994-10-25
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