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butyl cyclopropyl ether | 15786-41-1

中文名称
——
中文别名
——
英文名称
butyl cyclopropyl ether
英文别名
Butoxy-cyclopropan;butoxycyclopropane
butyl cyclopropyl ether化学式
CAS
15786-41-1
化学式
C7H14O
mdl
——
分子量
114.188
InChiKey
PGNSFKBGZSXHOJ-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:
    30 °C(Press: 20 Torr)
  • 密度:
    0.8066 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    8
  • 可旋转键数:
    4
  • 环数:
    1.0
  • 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

  • 作为产物:
    描述:
    乙烯基正丁醚二碘甲烷diethylzinc 作用下, 以 乙醚 为溶剂, 生成 butyl cyclopropyl ether
    参考文献:
    名称:
    通过烯烃与二烷基锌和亚甲基碘的反应合成环丙烷
    摘要:
    描述了一种通过烯烃与二烷基锌和亚甲基碘反应生成环丙烷的新颖合成途径。该反应的基本特征类似于Simmons-Smith反应的特征,该反应包括用亚甲基碘和锌-铜对处理烯烃。但是,该新方法更容易得到环丙烷,并且特别适合于将阳离子聚合性烯烃例如乙烯基醚转化为相应的环丙烷。当使用Simmons-Smith反应时,这类烯烃有时会因聚合反应而产生较低的环丙烷收率。
    DOI:
    10.1016/0040-4020(68)89007-6
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文献信息

  • 2-W-diaminocarboxylic acid compounds
    申请人:Rentzea Costin
    公开号:US20050085516A1
    公开(公告)日:2005-04-21
    2,ω-Diaminocarboxylic acid compounds of formula (I), where X, X 1 , Ar ω , Ar 2 and Y are as defined in claim 1, and their use as herbicides, are described.
    公式(I)中的2,ω-二氨基羧酸化合物,其中X,X1,Arω,Ar2和Y如权利要求1所定义,并描述了它们作为除草剂的用途。
  • BORON-CONTAINING SMALL MOLECULES
    申请人:Jarnagin Kurt
    公开号:US20120035132A1
    公开(公告)日:2012-02-09
    Compounds, pharmaceutical formulations, and methods of treating anti-inflammatory conditions and/or helminth-associated diseases are disclosed.
    本发明涉及化合物、药物配方和治疗抗炎症状况和/或寄生虫相关疾病的方法。
  • BICYCLIC HETEROCYCLIC DERIVATIVE
    申请人:Nakahira Hiroyuki
    公开号:US20110190278A1
    公开(公告)日:2011-08-04
    The present invention relates to a compound of the following formula (I) or a pharmaceutically acceptable salt thereof, being useful as a renin inhibitor. [wherein R 1a is halogen, etc.; R 1m is H, etc.; G 1 is —N(R 1b )—, etc.; G 2 is —CO—, etc.; G 3 is —C(R 1c )(R 1d )—, etc.; G 4 is oxygen, etc.; R 1b is optionally substituted C 1-6 alkyl, etc.; R 1c and R 1d are independently the same or different, H, etc.; R 3 is H, optionally substituted C 1-6 alkyl, etc.; R 3a , R 3b , R 3 c and R 3d are independently the same or different, and a group: -A-B (said A is single bond, etc., and said B is H, etc.), etc.; and n is 1, etc.]
    本发明涉及以下式(I)的化合物或其药学上可接受的盐,其可用作肾素抑制剂。[其中,R1a是卤素等;R1m是H等;G1是—N(R1b)—等;G2是—CO—等;G3是—C(R1c)(R1d)—等;G4是氧等;R1b是可选取代的C1-6烷基等;R1c和R1d独立选择为H等;R3是H、可选取代的C1-6烷基等;R3a、R3b、R3c和R3d独立选择为相同或不同的基团:-A-B(其中A是单键等,B是H等)等;n为1等。]
  • N-SUBSTITUTED-CYCLIC AMINO DERIVATIVE
    申请人:Suetsugu Satoshi
    公开号:US20120122773A1
    公开(公告)日:2012-05-17
    The present invention provides a compound of formula (I): wherein R 1a is optionally substituted C 1-6 alkyl, etc.; R 1m is hydrogen atom, etc.; G 1 , G 2 , G 3 and G 4 are (i), etc. ((i) G 1 is —N(R 1b )—, G 2 is —CO—, G 3 is —C(R 1c )(R 1d )—, and G 4 is oxygen, etc.); R 1b is optionally substituted C 1-6 alkyl, etc.; R 1c and R 1d are each independently optionally substituted C 1-6 alkyl, etc.; R 2 is optionally substituted C 1-6 alkyl, etc.; R 3a , R 3b , R 3c and R 3d are each independently a group: -A-B (A is a single bond, etc., B is hydrogen atom, etc.), etc.; n is 1, etc.; R 5 is C 1-4 alkoxycarbonyl, etc., or a pharmaceutically acceptable salt thereof, which is useful as a renin inhibitor.
    本发明提供了一种化合物,其化学式为(I):其中R1a是可选取代的C1-6烷基等;R1m是氢原子等;G1,G2,G3和G4是(i)等,((i) G1是—N(R1b)—,G2是—CO—,G3是—C(R1c)(R1d)—,G4是氧原子等);R1b是可选取代的C1-6烷基等;R1c和R1d分别独立地是可选取代的C1-6烷基等;R2是可选取代的C1-6烷基等;R3a、R3b、R3c和R3d分别独立地是一种基团:-A-B(其中A是单键等,B是氢原子等)等;n是1等;R5是C1-4烷氧羰基等,或其药学上可接受的盐,其作为一种肾素抑制剂是有用的。
  • Oxidation process of ethers
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP0878458A1
    公开(公告)日:1998-11-18
    An ether is oxidized with oxygen under an oxidation catalyst comprising an imide compound (such as N-hydroxyphthalimide) or the imide compound and a co-catalyst to produce the corresponding chain or cyclic ester or anhydride. The co-catalyst may be a transition metal compound. The above process provides a process for oxidizing an ether by oxygen efficiently to produce the corresponding oxide (such as an ester, an hydride) with high conversion and selectivity.
    醚在由亚胺化合物(如 N-羟基邻苯二甲酰亚胺)或亚胺化合物和助催化剂组成的氧化催化剂作用下与氧气氧化,生成相应的链状或环状酯或酸酐。助催化剂可以是过渡金属化合物。上述工艺提供了一种用氧气高效氧化醚的工艺,以高转化率和高选择性生成相应的氧化物(如酯、氢化物)。
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