摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

n-Hexyloxyessigsaeure-methylester | 70038-38-9

中文名称
——
中文别名
——
英文名称
n-Hexyloxyessigsaeure-methylester
英文别名
Methyl 2-hexoxyacetate
n-Hexyloxyessigsaeure-methylester化学式
CAS
70038-38-9
化学式
C9H18O3
mdl
——
分子量
174.24
InChiKey
KKQCNZLPPHGLBD-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:
    230.2±13.0 °C(Predicted)
  • 密度:
    0.932±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    12
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:2fe6a24276fab491eb9d9a777c342fcc
查看

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

反应信息

  • 作为反应物:
    描述:
    甲酸甲酯n-Hexyloxyessigsaeure-methylester万古霉素potassium tert-butylate 作用下, 以 乙醚N,N-二甲基甲酰胺 为溶剂, 反应 17.0h, 生成
    参考文献:
    名称:
    Design and synthesis of new vancomycin derivatives
    摘要:
    A set of vancomycin derivatives with lipid chain attached via a glyceric acid linker was designed and synthesized. A concise synthesis towards these derivatives was developed and the IC(50)s of these new lipoglycopeptides were tested. Some of them showed very potent activity against both vancomycin sensitive and resistant strains. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.03.093
  • 作为产物:
    描述:
    正己醇氯化亚砜 、 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 生成 n-Hexyloxyessigsaeure-methylester
    参考文献:
    名称:
    Design and synthesis of new vancomycin derivatives
    摘要:
    A set of vancomycin derivatives with lipid chain attached via a glyceric acid linker was designed and synthesized. A concise synthesis towards these derivatives was developed and the IC(50)s of these new lipoglycopeptides were tested. Some of them showed very potent activity against both vancomycin sensitive and resistant strains. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.03.093
点击查看最新优质反应信息

文献信息

  • Transition-metal-catalyzed reaction of diazocompounds, efficient synthesis of functionalized ethers by carbene insertion into the hydroxylic bond of alcohols
    作者:A.F. Noels、A. Demonceau、N. Petiniot、A.J. Hubert、Ph. Teyssié
    DOI:10.1016/0040-4020(82)80031-8
    日期:——
    An Efficient catalytic synthesis of unsaturated ethers by carbene insertion (with diazoesters as carbene precursors) into the OH bond of unsaturated alcohols is reported. The regioselectivity for the OH insertion is high. However, depending on the catalyst counter-ions and the diazoester alkoxy group, addition to the unsaturated centre can be promoted to some extent, yielding then cyclopropyl and cyclopropenyl
    据报道,通过将卡宾(以重氮酸酯作为卡宾的前体)插入不饱和醇的OH键,可以有效地催化合成不饱和醚。OH插入的区域选择性高。然而,取决于催化剂的抗衡离子和重氮酯烷氧基,可以在一定程度上促进向不饱和中心的加成,然后得到环丙基和环丙烯基甲醇。讨论了反应的机理。
  • 5-(M-CYANOBENZYLAMINO)PYRAZOLE DERIVATIVES
    申请人:Sankyo Company, Limited
    公开号:EP1304325A1
    公开(公告)日:2003-04-23
    Provided is a 5-(m-cyanobenzylamino)pyrazole derivative represented by the following formula:    wherein: R1 represents a C1-6 alkyl group, a C3-7 cycloalkyl group or a phenyl group; R2 represents a hydrogen atom or a C1-6 alkyl group; R3 represents a C1-6 alkyl, etc., R4 represents a hydrogen atom, a halogen atom, a C1-6 alkyl group, etc., Y represents a C1-6 alkyl group, etc.; and n is an integer of 0 to 4; or a salt thereof.
    本发明提供了由下式表示的 5-(间氰基苄基氨基)吡唑衍生物: 其中 R1代表C1-6烷基、C3-7环烷基或苯基; R2代表氢原子或C1-6烷基 R3 代表 C1-6 烷基等、 R4 代表氢原子、卤素原子、C1-6 烷基等、 Y 代表 C1-6 烷基等;以及 n 是 0 至 4 的整数; 或其盐。
  • Antifungal Properties of n-Alkoxyacetic Acids and Their Methyl Esters
    作者:Herman Gershon、Larry Shanks、Alan Deangelis
    DOI:10.1002/jps.2600680125
    日期:1979.1
  • NOELS, A. F.;DEMONCEAU, A.;PETINIOT, N.;HUBERT, A. J.;TEYSSIE, PH., TETRAHEDRON, 1982, 38, N 17, 2733-2739
    作者:NOELS, A. F.、DEMONCEAU, A.、PETINIOT, N.、HUBERT, A. J.、TEYSSIE, PH.
    DOI:——
    日期:——
  • Design and synthesis of new vancomycin derivatives
    作者:Wen Gu、Bei Chen、Min Ge
    DOI:10.1016/j.bmcl.2014.03.093
    日期:2014.5
    A set of vancomycin derivatives with lipid chain attached via a glyceric acid linker was designed and synthesized. A concise synthesis towards these derivatives was developed and the IC(50)s of these new lipoglycopeptides were tested. Some of them showed very potent activity against both vancomycin sensitive and resistant strains. (C) 2014 Elsevier Ltd. All rights reserved.
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物