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6-羟基-5-喹啉羧酸甲酯 | 104612-29-5

中文名称
6-羟基-5-喹啉羧酸甲酯
中文别名
——
英文名称
methyl 6-hydroxyquinolin-5-carboxylate
英文别名
6-Hydroxy-5-quinolinecarboxylic acid methyl ester;Methyl 6-hydroxyquinoline-5-carboxylate
6-羟基-5-喹啉羧酸甲酯化学式
CAS
104612-29-5
化学式
C11H9NO3
mdl
——
分子量
203.197
InChiKey
DKPAJWRNBBDOJR-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:
    342.5±22.0 °C(Predicted)
  • 密度:
    1.327±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    59.4
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:4183803e3ff42a62eb78bdf42adfa138
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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:
    参考文献:
    名称:
    Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur
    摘要:
    芳香族氮杂七元酮和硫醚的化学式为##STR1##其中;A为苯、萘、喹啉或吡啶;B为氧或硫;E为氧、硫或##STR2##n为1、2或3;Z为氨基或含氮杂环的基团;R为氢、较低烷基、环烷基或苯基较低烷基;Y为卤素、较低烷基、较低烷氧基、二较低烷基氨基、硝基、氨基、较低乙酰氨基、三氟甲基、苯基或被从卤素、较低烷基、较低烷氧基、二较低烷基氨基、硝基、氨基、较低酰胺基或三氟甲基中选择的一个至三个Y'基团取代的苯基;具有抗组胺作用,公开了其制备方法和化学中间体。
    公开号:
    US04705853A1
  • 作为产物:
    参考文献:
    名称:
    Fused aromatic oxazepinones, thiazepinones, diazepinones and sulfur
    摘要:
    公开了具有以下式子的芳香族氮杂环酮和硫酮:##STR1## 其中; A是苯,萘,喹啉或吡啶; B是氧或硫; E是氧,硫或##STR2## n为1,2或3; Z是氨基或含杂环氮的基团; R是氢,较低烷基,环烷基或苯基较低烷基; 具有抗组胺作用,公开了其制备方法和化学中间体。
    公开号:
    US04592866A1
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文献信息

  • Condensed heterocyclic derivatives and herbicides
    申请人:Kumiai Chemical Industry Co., Ltd.
    公开号:US05616537A1
    公开(公告)日:1997-04-01
    A condensed heterocyclic derivative of the formula (I): ##STR1## (wherein R is a hydroxyl group, R.sup.3 or R.sup.4 is an alkoxy group, W is an oxygen atom, Yn is a hydrogen atom, Z is a methine group, and A is a 5- or 6-membered heterocyclic ring which may be substituted, and a herbicide, are presented. When used for paddy field treatment, upland soil treatment and foliage treatment, the condensed heterocyclic derivative of the present invention exhibits excellent herbicidal activities against gramineous and non-gramineous weeds without adversely affecting crop plants.
    一种式(I)的缩合杂环衍生物:##STR1##(其中R为羟基,R.sup.3或R.sup.4为烷氧基,W为氧原子,Yn为氢原子,Z为甲川基,A为可被取代的5或6元杂环环),以及一种除草剂,被提出。当用于水稻田处理、旱地土壤处理和叶面处理时,本发明的缩合杂环衍生物对禾本科和非禾本科杂草表现出优异的除草活性,而对作物植物无不良影响。
  • Intermediates useful in the preparation of fused aromatic oxazepinones,
    申请人:A. H. Robins Company, Inc.
    公开号:US04727152A1
    公开(公告)日:1988-02-23
    Chemical intermediates having the formula: ##STR1## wherein A represents an aromatic or heterocyclic ring system selected from benzene, a naphthalene, a quinoline or a pyridine in any of its four positions, any of the rings systems are optionally substituted by one or two Y radicals selected from the group consisting of halo, loweralkyl, loweralkoxy, diloweralkylamino, nitro or trifluoromethyl; R is selected from the group consisting of loweralkyl, cycloalkyl or phenylloweralkyl wherein phenyl is optionally substituted by one or two radicals selected from halo, loweralkyl, loweralkoxy, nitro or trifluoromethyl; R.sup.4 and R.sup.5 are selected from hydrogen or loweralkyl; n is 1 or 2; X is selected from chlorine, bromine, or fluorine and E is selected from sulfur, oxygen or ##STR2## and chemical intermediates having the formula: ##STR3## wherein A, R, R.sup.4, R.sup.5, E and n are as defined above and Q is selected from the group consisting of ##STR4## wherein R.sup.3 is hydrogen, an acid neutralizing ion or an esterifying radical; with the proviso that when n is 2 and E is oxygen, A is other than phenyl or substituted phenyl. These chemical intermediates are useful in the preparation of oxazepinones, thiazepinones and diazepinones which exhibit antihistaminic activity.
    化学中间体的化学式为:##STR1## 其中A代表苯、萘、喹啉或吡啶中的任意一个芳香或杂环环系,在任何四个位置上选择,任何一个环系都可以选择由卤、低烷基、低烷氧基、二低烷基氨基、硝基或三氟甲基中的一个或两个Y基团取代;R选自低烷基、环烷基或苯基低烷基,其中苯基可以选择由卤、低烷基、低烷氧基、硝基或三氟甲基中的一个或两个基团取代;R.sup.4和R.sup.5选自氢或低烷基;n为1或2;X选择氯、溴或氟,E选择硫、氧或##STR2## 化学中间体的化学式为:##STR3## 其中A、R、R.sup.4、R.sup.5、E和n的定义如上所述,Q选择##STR4## 其中R.sup.3为氢、酸中和离子或酯化基团;但当n为2且E为氧时,A不是苯或取代苯。这些化学中间体在制备具有抗组胺活性的噁唑烷酮、噻唑烷酮和二嗪烷酮方面非常有用。
  • Certain 2,5 and 2,5,6-di- and tri-substituted nicotinic acid
    申请人:A. H. Robins Company, Incorporated
    公开号:US04810795A1
    公开(公告)日:1989-03-07
    Aromatic azepinones and thiones having the formula ##STR1## wherein; A is benzene, naphthalene, quinoline or pyridine; B is oxygen or sulfur; ##STR2## E is oxygen, sulfur or n is 1, 2 or 3; Z is an amino or a heterocyclic nitrogen-containing radical; R is hydrogen, loweralkyl, cycloalkyl or phenyl-loweralkyl; Y is halo, loweralkyl, loweralkoxy, diloweralkylamino, nitro, amino, loweracetylamino, trifluoromethyl, phenyl or phenyl substituted by one to three Y' radicals selected from halo, loweralkyl, loweralkoxy, diloweralkylamino, nitro, amino, loweracylamino or trifluoromethyl; and having antihistaminic utility, a process for the preparation thereof and chemical intermediates therefor are disclosed.
    公开了具有以下公式的芳香族氮杂七元酮和硫酮:##STR1## 其中;A为苯,萘,喹啉或吡啶;B为氧或硫;##STR2## E为氧,硫或n为1、2或3;Z为氨基或含氮杂环的杂环基;R为氢,低烷基,环烷基或苯基-低烷基;Y为卤素,低烷基,低烷氧基,二低烷基氨基,硝基,氨基,低乙酰氨基,三氟甲基,苯基或由一到三个Y'基选择的卤素,低烷基,低烷氧基,二低烷基氨基,硝基,氨基,低乙酰氨基或三氟甲基取代的苯基;具有抗组胺作用,公开了其制备方法和化学中间体。
  • CONDENSED HETEROCYCLIC DERIVATIVE AND WEEDKILLER
    申请人:KUMIAI CHEMICAL INDUSTRY CO., LTD.
    公开号:EP0606489A1
    公开(公告)日:1994-07-20
    A condensed heterocyclic derivative represented by general formula (I) and a weedkiller, wherein R represents hydroxy, R³ and R⁴ represent each alkoxy, W represents oxygen, Yn represents hydrogen, Z represents methine, and A represents a 5- or 6-membered heterocyclic group which may be substituted. The derivative does not injure crops in the water treatment in a paddy field, upland farming, soil treatment and foliage treatment, and has an excellent weedkilling activity against gramineous and nongramineous weeds.
    一种由通式(I)代表的缩合杂环衍生物和一种除草剂,其中 R 代表羟基,R³ 和 R⁴ 分别代表烷氧基,W 代表氧,Yn 代表氢,Z 代表甲烷,A 代表可被取代的 5 或 6 元杂环基团。该衍生物在水田水处理、高地耕作、土壤处理和叶面处理中不会伤害作物,对禾本科杂草和非禾本科杂草具有优异的除草活性。
  • US4592866A
    申请人:——
    公开号:US4592866A
    公开(公告)日:1986-06-03
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