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dodecyl-octyl ether | 36339-51-2

中文名称
——
中文别名
——
英文名称
dodecyl-octyl ether
英文别名
Dodecyl-octyl-aether;octyl dodecanol;Dodecyl octyl ether;1-octoxydodecane
dodecyl-octyl ether化学式
CAS
36339-51-2
化学式
C20H42O
mdl
——
分子量
298.553
InChiKey
MMMPXNOKIZOWHM-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):
    9.1
  • 重原子数:
    21
  • 可旋转键数:
    18
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

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文献信息

  • ANTI-TUMOR EFFECT POTENTIATOR
    申请人:Fukuoka Masayoshi
    公开号:US20120225838A1
    公开(公告)日:2012-09-06
    There is provided an agent for potentiating the effects of an anti-tumor agent. An anti-tumor effect potentiator containing, as an active ingredient, a uracil compound represented by the following formula (I) or a pharmaceutically acceptable salt thereof: wherein X represents a C 1-5 alkylene group and one of methylene groups constituting the alkylene group is optionally substituted with an oxygen atom; R 1 represents a hydrogen atom or a C 1-6 alkyl group; R 2 represents a hydrogen atom or a halogen atom; and R 3 represents a C 1-6 alkyl group, a C 2-6 alkenyl group, a C 3-6 cycloalkyl group, a (C 3-6 cycloalkyl) C 1-6 alkyl group, a halogeno-C 1-6 alkyl group or a saturated heterocyclic group.
    提供了一种用于增强抗肿瘤药物效果的药剂。 一种抗肿瘤效应增强剂,其包含以下式(I)所代表的尿嘧啶化合物或其药用可接受的盐作为活性成分: 其中X代表一个C1-5烷基基团,构成该烷基基团的亚甲基基团之一可以选择性地被氧原子取代; R1代表氢原子或一个C1-6烷基基团;R2代表氢原子或卤原子;R3代表一个C1-6烷基基团,一个C2-6烯基基团,一个C3-6环烷基基团,一个(C3-6环烷基)C1-6烷基基团,一个卤代C1-6烷基基团或一个饱和杂环基团。
  • Cyclic diamine compound with condensed-ring groups
    申请人:Kowa Co., Ltd.
    公开号:US20030060461A1
    公开(公告)日:2003-03-27
    A cyclic diamine compound of formula (1): 1 wherein R 1 and R 2 are individually a hydrogen atom or a methoxy group, provided R 1 is a methoxy group when R 2 is a hydrogen atom, or a hydrogen atom when R 2 is a methoxy group; A is an oxygen atom, a sulfur atom, CH═CH, CH═N or NR 3 , in which R 3 is a hydrogen atom, or a lower alkyl, hydroxy lower alkyl, lower alkoxy lower alkyl, aryl or aryl lower alkyl group; B is a nitrogen atom, CH or CR 4 , in which R 4 is a hydrogen atom, or a lower alkyl, hydroxy lower alkyl, lower alkoxy lower alkyl, aryl or aryl lower alkyl group; m is 1 or 2; and n is a number of 1 to 5, an acid-addition salt thereof, or a hydrate thereof. The compound has inhibitory effects on cell adhesion and is useful for treatment of allergy, asthma, rheumatism, arteriosclerosis, and inflammation.
    公式(1)所示的环状二胺化合物:1 其中R1和R2分别是个别氢原子或甲氧基,条件是当R2是氢原子时R1是甲氧基,或者当R2是甲氧基时R1是氢原子;A是氧原子、硫原子、CH═CH、CH═N或NR3,其中R3是氢原子,或者是低级烷基、羟基低级烷基、低级烷氧基低级烷基、芳基或芳基低级烷基团;B是氮原子、CH或CR4,其中R4是氢原子,或者是低级烷基、羟基低级烷基、低级烷氧基低级烷基、芳基或芳基低级烷基团;m是1或2;n是1到5的数字,其酸加成盐,或其水合物。该化合物具有抑制细胞粘附的作用,并且对于治疗过敏、哮喘、风湿病、动脉硬化以及炎症是有用的。
  • Cyclic amine compounds and pharmaceutical composition containing the same
    申请人:KOWA CO., LTD.
    公开号:US20040010147A1
    公开(公告)日:2004-01-15
    A cyclic amine compound represented by the following general formula (1): 1 wherein, R 1 , R 2 and R 3 each independently represent a hydrogen atom or an alkoxy group; W 1 and W 2 each independently represent N or CH; X represents O, NR 4 , CONR 4 or NR 4 CO; R 4 represents a hydrogen atom, or an alkyl, aryl, heteroaryl, aralkyl, or heteroaralkyl group; and l, m and n each represents a number of 0 or 1, a salt thereof and a hydrate thereof are provided. These compounds have inhibitory effects on both cell adhesion and cell infiltration and are useful as anti-asthmatic agents, anti-allergic agents, anti-rheumatic agents, anti-arteriosclerotic agents, anti-inflammatory agents, anti-Sjogren's syndrome agents or the like.
    以下是通用公式(1)表示的一个环胺化合物: 其中, R 1 ,R 2 和R 3 分别独立地表示氢原子或烷氧基; W 1 和W 2 分别独立地表示N或CH; X表示O,NR 4 ,CONR 4 或NR 4 CO; R 4 表示氢原子,或烷基,芳基,杂芳基,芳基烷基或杂芳基烷基; l,m和n分别表示0或1的数字, 提供其盐和水合物。 这些化合物对细胞粘附和细胞浸润均具有抑制作用,并可用作抗哮喘剂,抗过敏剂,抗风湿剂,抗动脉硬化剂,抗炎剂,抗干燥综合征剂等。
  • CARBINOL DERIVATIVES HAVING HETEROCYCLIC LINKER
    申请人:Koura Minoru
    公开号:US20100280013A1
    公开(公告)日:2010-11-04
    [Object] It is to provide a novel LXRβ agonist useful as a preventative and/or therapeutic agent for atherosclerosis; arteriosclerosis such as those resulting from diabetes; dyslipidemia; hypercholesterolemia; lipid-related diseases; inflammatory diseases that are caused by inflammatory cytokines; skin diseases such as allergic skin diseases; diabetes; or Alzheimer's disease. [Solving Means] A carbinol compound represented by the following general formula (I) or salt thereof, or their solvate: (wherein, each V and W independently show N or C—R 7 ; each X and Y independently show CH 2 , C═O, SO 2 , etc; Z shows CH or N; each R 1 , R 2 and R 7 independently show a hydrogen atom, C 1-8 alkyl group, etc.; R 3 shows C 1-8 alkyl group; R 4 shows an optionally substituted C 6-10 aryl group or an optionally substituted 5- to 11-membered heterocyclic group; R 5 and R 6 show a hydrogen atom, etc.; L shows a C 1-8 alkyl chain optionally substituted with an oxo group, etc.; and n shows any integer of 0 to 2.)
    它是提供一种新型的LXRβ激动剂,可用作预防和/或治疗动脉粥样硬化;动脉硬化,如由糖尿病引起的动脉硬化;血脂异常;高胆固醇血症;与脂质相关的疾病;由炎性细胞因子引起的炎症性疾病;过敏性皮肤病;糖尿病;或阿尔茨海默病的预防和/或治疗剂。【解决手段】由以下一般式(I)表示的羟甲基化合物或其盐,或它们的溶剂化合物: (其中,每个V和W独立地表示N或C—R 7 ;每个X和Y独立地表示CH 2 ,C═O,SO 2 等;Z表示CH或N;每个R 1 ,R 2 和R 7 独立地表示氢原子,C 1-8 烷基基团等;R 3 表示C 1-8 烷基基团;R 4 表示可选择地取代的C 6-10 芳基基团或可选择地取代的5-至11-成员杂环基团;R 5 和R 6 表示氢原子等;L表示可选择地取代有氧基团等的C 1-8 烷基链;n表示0至2的任意整数。】
  • NOVEL CONDENSED PYRIDINE OR CONDENSED PYRIMIDINE DERIVATIVE, AND MEDICINAL AGENT COMPRISING SAME
    申请人:Morimoto Toshiharu
    公开号:US20130102621A1
    公开(公告)日:2013-04-25
    The present invention relates to provision of a novel compound that has an activity of promoting insulin secretion from pancreatic β cells and thus is useful as a prophylaxis and/or therapeutic agent for diseases caused by hyperglycemia such as diabetes mellitus, and the compound represented by the following formula (1): wherein one of A and B represents a nitrogen atom and the other represents a nitrogen atom or CR 10 , X represents an oxygen atom, a sulfur atom or —(CH 2 )n-N(R 12 )—, Y represents an oxygen atom, a sulfur atom or —N(R 13 )—, and R 1 to R 9 each represent a hydrogen atom or another substituent, or a salt thereof, or a solvate of the compound or the salt.
    本发明涉及提供一种新型化合物,该化合物具有促进胰岛素从胰岛β细胞分泌的活性,因此可用作预防和/或治疗由高血糖引起的疾病,如糖尿病,所述化合物由以下式(1)表示: 其中A和B中的一个代表氮原子,另一个代表氮原子或CR10,X代表氧原子、硫原子或—(CH2)n-N(R12)—,Y代表氧原子、硫原子或—N(R13)—,R1至R9各自代表氢原子或另一取代基,或其盐,或该化合物或其盐的溶剂化合物。
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