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1-chloropentanol

中文名称
——
中文别名
——
英文名称
1-chloropentanol
英文别名
chloropentanol;1-chloropentan-1-ol
1-chloropentanol化学式
CAS
——
化学式
C5H11ClO
mdl
——
分子量
122.595
InChiKey
ZZZXZQQRTBBNHT-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):
    2.1
  • 重原子数:
    7
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

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文献信息

  • Benzimidazole compound
    申请人:Miyazawa Shuhei
    公开号:US20070010542A1
    公开(公告)日:2007-01-11
    An object of the present invention is to provide a novel chemical compound useful as a therapeutic or prophylactic agent for acid-related diseases, having an excellent inhibitory effect against gastric acid secretion, an excellent effect of maintaining the inhibitory effect against gastric acid secretion, thereby maintaining intragastric pH high for a long time, and having more safety and appropriate physicochemical stability. Provided is a compound represented by where R 1 and R 3 may be the same or different and each represent a hydrogen atom or a C1-C6 alkyl group; R 2 represents (5,5-dimethyl-1,3-dioxan-2-yl)methoxy group, 5,7-dioxaspiro[2.5]oct-6-ylmethoxy group, 1,5,9-trioxaspiro[5.5]undec-3-ylmethoxy group, or (2,2-dimethyl-1,3-dioxan-5-yl)methoxy group; R 4 , R 5 , R 6 and R 7 represent a hydrogen atom, halogen atom, C1-C6 alkyl group, C1-C6 haloalkyl group, C1-C6 alkoxy group or C1-C6 haloalkoxy group; and W 1 represents a single bond, methylene or ethylene group, a salt thereof or a solvate of these.
    本发明的目的是提供一种新型化合物,可用作治疗或预防酸相关疾病的药物,具有出色的抑制胃酸分泌作用,保持抑制胃酸分泌作用的出色效果,从而长时间保持胃内pH值高,并具有更高的安全性和适当的理化稳定性。 提供的化合物表示为 其中R 1 和R 3 可以相同也可以不同,每个代表氢原子或C1-C6烷基;R 2 表示(5,5-二甲基-1,3-二氧杂环戊烷-2-基)甲氧基基团,5,7-二氧杂螺[2.5]辛-6-基甲氧基基团,1,5,9-三氧杂螺[5.5]十一烷-3-基甲氧基基团,或(2,2-二甲基-1,3-二氧杂环戊烷-5-基)甲氧基基团; R 4 ,R 5 ,R 6 和R 7 代表氢原子,卤原子,C1-C6烷基,C1-C6卤代烷基,C1-C6烷氧基或C1-C6卤代烷氧基;W 1 表示单键,亚甲基或乙烯基,其盐或这些的溶剂化合物。
  • [EN] 1-(4-(ISOXAZOL-5-YL)-1H-PYRAZOL-1-YL)-2-METHYLPROPAN-2-OL DERIVATIVES AND RELATED COMPOUNDS AS IL-17 AND IFN-GAMMA INHIBITORS FOR TREATING AUTOIMMUNE DISEASES AND CHRONIC INFLAMMATION<br/>[FR] DÉRIVÉS DE 1-(4-(ISOXAZOL-5-YL)-1 H-PYRAZOL-1-YL)-2-MÉTHYLPROPAN-2-OL ET COMPOSÉS APPARENTÉS EN TANT QU'INHIBITEURS D'IL-17 ET D'IFN-GAMMA POUR LE TRAITEMENT DE MALADIES AUTO-IMMUNES ET D'UNE INFLAMMATION CHRONIQUE
    申请人:IMMUNIC AG
    公开号:WO2019048541A1
    公开(公告)日:2019-03-14
    The present invention relates to compounds of the general formula (I), and the pharmaceutically acceptable salts and solvates thereof, wherein Ar, Z and Y are as described herein and R1 is a group of the structure (formula (II)), wherein n is 0 or 1; R2 is H, deuterium or methyl; R3 is methyl, trilluoromethyl, ethyl, or taken with R2 together forms a cyclopropyl group, or R3 forms a methylene bridge to the carbon atom marked *, which are suitable for the treatment of autoimmune diseases and chronic inflammation.
    本发明涉及具有通用公式(I)的化合物,以及其中Ar、Z和Y如本文所述的药用可接受盐和溶剂化物,其中R1是具有结构(公式(II))的组,其中n为0或1;R2是H,氘或甲基;R3是甲基,三氟甲基,乙基,或者与R2共同形成一个环丙基组,或者R3形成一个甲基桥接到标记为*的碳原子上,这些化合物适合用于治疗自身免疫性疾病和慢性炎症。
  • Perfluoroalkylated aniline compound and process for producing the same
    申请人:——
    公开号:US20020198399A1
    公开(公告)日:2002-12-26
    The present invention provides an aniline derivative represented by the formula (I) 1 wherein R 1 and R 2 are each H, (C 1-12 )alkyl, (C 3-8 )cycloalkyl, hydroxy(C 1-12 )alkyl, hydroxycarbonyl (C 1-12 )alkyl, (C 1-6 )-alkoxycarbonyl(C 1-6 )alkyl, —COR 8 , wherein R 8 is H, halo-(C 1-12 )alkyl, (C 3-8 )cycloalkyl or (substituted) phenyl, COOR 9 , wherein R 9 is a halo(C 1-6 )alkyl group, (substituted) phenyl or (substituted) benzyl; R 3 , R 4 , R 5 , R 6 and R 7 are each H, halogen, OH, nitro, halo(C 1-12 )alkylthio, (substituted)amino-(C 1-2 )alkyl, (substituted) phenyl, (substituted) benzyl, amino, —N(R 10 )R 11 wherein R 10 and R 11 are each H, alkyl, cycloalkyl, (substituted) phenyl, (substituted) benzyl, —COR 8 or COOR 9 , or (C 2-27 )perfluoroalkyl, etc., and a process for producing the aniline derivative. According to the process of the present invention, perfluoroalkylaniline derivatives can be obtained by using various anilines as the substrate with a high position selectivity and high yield.
    本发明提供了一种由公式(I)表示的苯胺衍生物: 1 其中R 1 和R 2 各自是H,(C 1-12 )烷基,(C 3-8 )环烷基,羟基(C 1-12 )烷基,羟甲氧基(C 1-12 )烷基,(C 1-6 )-烷氧甲氧基(C 1-6 )烷基,—COR 8 ,其中R 8 是H,卤代-(C 1-12 )烷基,(C 3-8 )环烷基或(取代)苯基,COOR 9 ,其中R 9 是卤代(C 1-6 )烷基,(取代)苯基或(取代)苄基;R 3 ,R 4 ,R 5 ,R 6 和R 7 各自是H,卤素,OH,硝基,卤代-(C 1-12 )烷基硫,(取代)氨基-(C 1-2 )烷基,(取代)苯基,(取代)苄基,氨基,—N(R 10 )R 11 ,其中R 10 和R 11 各自是H,烷基,环烷基,(取代)苯基,(取代)苄基,—COR 8 或COOR 9 ,或(C 2-27 )全氟烷基等,以及一种用于生产该苯胺衍生物的过程。根据本发明的过程,可以通过使用各种苯胺作为底物,以高位置选择性和高收率获得全氟烷基苯胺衍生物。
  • [EN] 5-ARYL ISOXAZOLINES FOR CONTROLLING PESTS<br/>[FR] 5-ARYL-ISOXAZOLINES POUR LUTTER CONTRE LES NUISIBLES
    申请人:NOVARTIS AG
    公开号:WO2011157748A1
    公开(公告)日:2011-12-22
    The invention relates to new isoxazoline compounds of formula (I) wherein the variables have the meaning as indicated in the claims; in free form and in salt form; and optionally the enantiomers and geometrical isomers thereof. The compounds of formula (I) are useful in the control of parasites, in particular ectoparasites, in and on vertebrates.
    本发明涉及新的异恶唑啉化合物,其化学式为(I),其中变量具有如权利要求中所指出的含义;以自由形式和盐形式存在;以及可选地包括它们的对映异构体和几何异构体。公式(I)的化合物在控制脊椎动物内外的寄生虫,特别是外寄生虫方面是有用的。
  • Heterocyclyl-substituted benzoylcyclohexandiones, their preparation, and their use as herbicides
    申请人:——
    公开号:US20020173424A1
    公开(公告)日:2002-11-21
    There are described benzoylcyclohexanediones of the formula I, their preparation, and their use as herbicides and plant growth regulators. 1 In this formula (I), R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R a , R b and R c are various radicals, and Y and Z are a monoatomic bridge element.
    该公式描述了式I的苯甲酰环己二酮,它们的制备以及它们作为除草剂和植物生长调节剂的用途。 在这个公式(I)中,R1,R2,R3,R4,R5,R6,R7,Ra,Rb和Rc是各种基团,Y和Z是单原子桥元素。
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