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4,4-二甲基环己烷羰基氯化物 | 220203-29-2

中文名称
4,4-二甲基环己烷羰基氯化物
中文别名
——
英文名称
4,4-dimethyl-cyclohexanecarbonyl chloride
英文别名
4,4-Dimethylcyclohexane-1-carbonyl chloride
4,4-二甲基环己烷羰基氯化物化学式
CAS
220203-29-2
化学式
C9H15ClO
mdl
——
分子量
174.671
InChiKey
ZZZNOUIVXGCQBY-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):
    3.5
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:17f94a4a1f3df206886813b54506cc8a
查看

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Studies on hypolipidemic agents. V. Synthesis and esterase-inhibitory activity of 2-(1,4- and 4,4-dialkylcyclohexyl)-2-oxoethyl arenesulfonates.
    摘要:
    合成了 2-(1,t- 和 c-4-二烷基环己-r-1-基)-2-氧代乙基异辛烷磺酸盐、2-(4,4-二烷基环己-1-基)-2-氧代乙基异辛烷磺酸盐和相关化合物,并对其体外酯酶和糜蛋白酶抑制活性以及体内降血脂作用进行了评估。2-(1, 4-二烷基环己-1-基)-2-氧代乙基甲磺酸酯的反式异构体显示出比顺式异构体更强的酯酶抑制作用(约 13 至 6200 倍)以及更强的降血脂作用(约 1.5 至 10 倍),但这两种异构体的糜蛋白酶抑制作用同样较低。另一方面,具有 4,4- 二取代环己烷环的 2-氧代乙基异磺酸盐大多具有强效的酯酶抑制作用(按 IC50 的顺序排列;10-8 至 10-9M)和明显的降血脂作用(血浆甘油三酯降低 78% 至 95%)。
    DOI:
    10.1248/cpb.35.4130
  • 作为产物:
    参考文献:
    名称:
    Studies on hypolipidemic agents. V. Synthesis and esterase-inhibitory activity of 2-(1,4- and 4,4-dialkylcyclohexyl)-2-oxoethyl arenesulfonates.
    摘要:
    合成了 2-(1,t- 和 c-4-二烷基环己-r-1-基)-2-氧代乙基异辛烷磺酸盐、2-(4,4-二烷基环己-1-基)-2-氧代乙基异辛烷磺酸盐和相关化合物,并对其体外酯酶和糜蛋白酶抑制活性以及体内降血脂作用进行了评估。2-(1, 4-二烷基环己-1-基)-2-氧代乙基甲磺酸酯的反式异构体显示出比顺式异构体更强的酯酶抑制作用(约 13 至 6200 倍)以及更强的降血脂作用(约 1.5 至 10 倍),但这两种异构体的糜蛋白酶抑制作用同样较低。另一方面,具有 4,4- 二取代环己烷环的 2-氧代乙基异磺酸盐大多具有强效的酯酶抑制作用(按 IC50 的顺序排列;10-8 至 10-9M)和明显的降血脂作用(血浆甘油三酯降低 78% 至 95%)。
    DOI:
    10.1248/cpb.35.4130
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文献信息

  • SULFUR-CONTAINING BICYCLIC COMPOUND
    申请人:Astellas Pharma Inc.
    公开号:US20150111876A1
    公开(公告)日:2015-04-23
    A sulfur-containing bicyclic compound having a PAM action of GABA B , and it use for preventing and/or treating schizophrenia, CIAS, cognitive impairment, fragile X syndrome, autism spectrum disorder, spasticity, anxiety disorder, substance addiction, pain, fibromyalgia, or Charcot-Marie-Tooth disease. A pharmaceutical composition for preventing and/or treating schizophrenia, cognitive impairment associated with schizophrenia (CIAS), cognitive impairment, fragile X syndrome, autism spectrum disorder, spasticity, anxiety disorder, substance addiction, pain, fibromyalgia, Charcot-Marie-Tooth disease, or the like, which has a positive allosteric modulator (PAM action) of GABA B .
    一种含硫的双环化合物,具有GABAB的PAM作用,用于预防和/或治疗精神分裂症、CIAS、认知障碍、脆性X综合征、自闭症谱系障碍、痉挛、焦虑症、物质成瘾、疼痛、纤维肌痛或沙科-玛丽-托斯病。一种用于预防和/或治疗精神分裂症、与精神分裂症相关的认知障碍(CIAS)、认知障碍、脆性X综合征、自闭症谱系障碍、痉挛、焦虑症、物质成瘾、疼痛、纤维肌痛、沙科-玛丽-托斯病等的药物组合物,具有GABAB的正向变构调节剂(PAM作用)。
  • Sulfonic acid ester derivatives useful as antilipemic agents
    申请人:Taiho Pharmaceutical Company, Limited
    公开号:US04675428A1
    公开(公告)日:1987-06-23
    A sulfonic acid ester derivative represented by the general formula ##STR1## wherein R.sub.1 is a hydrogen atom, alkyl having 1 to 4 carbon atoms or alkoxy having 1 to 4 carbon atoms, A is a group represented by the general formula ##STR2## (wherein R.sub.2 and R.sub.3 are each alkyl having 1 to 4 carbon atoms) or by the general formula ##STR3## (wherein R.sub.4 and R.sub.5 are each alkyl having 1 to 4 carbon atoms or, when taken together with the cabon atom to which they are attached, form cycloalkyl having 4 to 6 carbon atoms), and l is an integer of from 1 to 3, and a process for preparing the derivative.
    一种磺酸酯衍生物,其通式表示为 ##STR1## 其中R.sub.1为氢原子,具有1至4个碳原子的烷基或1至4个碳原子的烷氧基,A是由通式##STR2##(其中R.sub.2和R.sub.3均为具有1至4个碳原子的烷基)或由通式##STR3##(其中R.sub.4和R.sub.5均为具有1至4个碳原子的烷基或与它们所连接的碳原子一起形成具有4至6个碳原子的环烷基),l为1至3的整数,以及制备该衍生物的方法。
  • Sulfonic acid ester derivatives and process for preparing same
    申请人:Taiho Pharmaceutical Company Limited
    公开号:US04797502A1
    公开(公告)日:1989-01-10
    A sulfonic acid ester derivative represented by the general formula ##STR1## wherein R.sub.1 is a hydrogen atom, alkyl having 1 to 4 carbon atoms or alkoxy having 1 to 4 carbon atoms, A is a group represented by the general formula ##STR2## (wherein R.sub.2 and R.sub.3 are each alkyl having 1 to 4 carbon atoms) or by the general formula ##STR3## (wherein R.sub.4 and R.sub.5 are each alkyl having 1 to 4 carbon atoms or, when taken together with the carbon atom to which they are attached, form cycloalkyl having 4 to 6 carbon atoms), and l is an integer of from 1 to 3, and a process for preparing the derivative.
    一种磺酸酯衍生物,其通式表示为##STR1##其中R.sub.1是氢原子,具有1至4个碳原子的烷基或具有1至4个碳原子的烷氧基,A是由通式##STR2## (其中R.sub.2和R.sub.3均为具有1至4个碳原子的烷基)或由通式##STR3## (其中R.sub.4和R.sub.5均为具有1至4个碳原子的烷基或与它们附着的碳原子一起形成具有4至6个碳原子的环烷基)表示的基团,l为1至3的整数,并提供了制备该衍生物的方法。
  • 2' and 3'-nucleoside prodrugs for treating Flaviviridae infections
    申请人:Gosselin Gilles
    公开号:US20070042990A1
    公开(公告)日:2007-02-22
    2′ and 3′-Prodrugs of 1′, 2′, 3′ or 4′-branched β-D or β-L nucleosides, or their pharmaceutically acceptable salts and derivatives are described, which are useful in the prevention and treatment of Flaviviridae infections and other related conditions. These modified nucleosides provide superior results against flaviviruses and pestiviruses, including hepatitis C virus and viruses generally that replicate through an RNA dependent RNA reverse transcriptase. Compounds, compositions, methods and uses are provided for the treatment of Flaviviridae infection, including HCV infection, that include the administration of an effective amount of the prodrugs of the present invention, or their pharmaceutically acceptable salts or derivatives. These drugs may optionally be administered in combination or alteration with further anti-viral agents to prevent or treat Flaviviridae infections and other related conditions.
    本文介绍了1'、2'、3'或4'-支链β-D或β-L核苷的2'和3'-前药,或其药学上可接受的盐和衍生物。这些修饰核苷对黄病毒科感染和其他相关病症的预防和治疗具有优越的效果。这些化合物提供了优越的结果,可抵抗黄病毒和猪瘟病毒,包括C型肝炎病毒和通过RNA依赖性RNA逆转录酶复制的病毒。本发明提供了用于治疗黄病毒科感染,包括HCV感染的化合物、组合物、方法和用途,其中包括对本发明的前药或其药学上可接受的盐或衍生物的有效剂量的给药。这些药物可以选择与其他抗病毒药物组合或交替使用,以预防或治疗黄病毒科感染和其他相关病症。
  • SULFONIC ESTER DERIVATIVES AND PROCESS FOR THEIR PREPARATION
    申请人:TAIHO PHARMACEUTICAL COMPANY LIMITED
    公开号:EP0117876A1
    公开(公告)日:1984-09-12
    Sulfonic ester derivatives represented by generalformu- la (I), wherein R, represents hydrogen, C1-4 alkyl or C-4 alkoxy, A represents (II), (wherein R2 and R3 each represent C1-4 alkyl) or (III), (wherein R4 and R5 each represent C1-4 alkyl, or they may be connected to each other to form C4-6 cycloalkyl together with the adjacent carbon atom), and represents an integer of 1 to 3, and a process for their preparation.
    由通式la(I)代表的磺酸酯衍生物,其中R代表氢、C1-4烷基或C-4烷氧基,A代表(II),(其中R2和R3各自代表C1-4烷基)或(III),(其中R4和R5各自代表C1-4烷基,或它们可以相互连接,与相邻碳原子一起形成C4-6环烷基),并代表1至3的整数,及其制备方法。
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