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methyl trans-pent-2-enyl carbonate | 101226-85-1

中文名称
——
中文别名
——
英文名称
methyl trans-pent-2-enyl carbonate
英文别名
α-Ethyl-crotonsaeure;Methyl (2E)-2-ethyl-2-butenoate;methyl (E)-2-ethylbut-2-enoate
methyl trans-pent-2-enyl carbonate化学式
CAS
101226-85-1
化学式
C7H12O2
mdl
——
分子量
128.171
InChiKey
URKOXBDVSBIUED-GQCTYLIASA-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):
    1.7
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    methyl trans-pent-2-enyl carbonate二乙胺 在 bis(1,5-cyclooctadiene)diiridium(I) dichloride 、 (1,1'-dinaphthyl-2,2'-diyl)-N,N'-di(Ph)(Et)phosphoramidite 作用下, 以 四氢呋喃 为溶剂, 反应 12.0h, 生成 Diethyl-α-ethylallylamin 、 3-Diethylamino-penten-2
    参考文献:
    名称:
    具有杂原子官能团的试剂中烷基的甲基 CH 键的区域特异性官能化
    摘要:
    我们报告了具有现有功能的分子中饱和末端 CH 键的区域特异性、铑催化硼化。使用过量的有机底物并作为限制试剂获得中等至良好的产率。三烷基胺、受保护的醇、受保护的酮和氟代烷烃的硼酸化发生在空间位阻最小的甲基上。还进行了探测对烷基硼化的电子效应的反应。这些反应表明硼酸化优先发生在最缺电子的甲基上。还开发了进行 CH 键串联硼酸化和将所得硼酸酯转化为醇、烷基芳烃和烷基三氟硼酸酯的方法。
    DOI:
    10.1021/ja044933x
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文献信息

  • ANTIBACTERIAL COMPOUNDS AND METHODS FOR USE
    申请人:PTC THERAPEUTICS, INC.
    公开号:US20150038437A1
    公开(公告)日:2015-02-05
    The present description relates to compounds and forms and pharmaceutical compositions thereof and methods for use thereof to treat or ameliorate bacterial infections caused by wild-type and multi-drug resistant Gram-negative and Gram-positive pathogens.
    本说明涉及化合物和形式以及其制药组合物,以及使用它们治疗或改善由野生型和多重耐药革兰氏阴性和革兰氏阳性病原体引起的细菌感染的方法。
  • GOUZOULES F. H.; WHITNEY R. A., J. ORG. CHEM., 51,(1986) N 11, 2024-2030
    作者:GOUZOULES F. H.、 WHITNEY R. A.
    DOI:——
    日期:——
  • COMPOSITION OF MATTER
    申请人:University of Louisiana at Lafayette
    公开号:US20170361310A1
    公开(公告)日:2017-12-21
    The method relates to the field of asymmetric allylic amination and comprises preparing a chiral N-substituted allylic amine compound from the corresponding allylic substrates and substituted hydroxylamines, in the presence of a catalyst, said catalyst comprising copper compounds and a chiral ligand. Examples of chiral amine compounds which can be made using the method include Vigabatrin, Ezetimibe Terbinafine, Naftifine 3-methylmorphine, Sertraline, Cinacalcet, Mefloquine hydrochloride, and Rivastigmine. There are over 20,000 known bioactive molecules with chiral N-substituted allylic amine substructure. The method may also be used to produce non-natural chiral β-aminoacid esters, a sub-class of chiral N-substituted allylic amine compounds. Examples of β-aminoacid ester which can be produced by the disclosed method, include, but are not limited to, N-(2-methylpent-1-en-3-yl)benzenamine and Ethyl 2-methylene-3-(phenylamino)butanoate. Further, the products of the method described herein can be used to produce chiral heterocycles and bioactive molecules or materials. A novel chiral copper-ligand nitrosoarene complex is also set forth.
  • ALKALINE AGENT FOR LIGHTENING HAIR CONTAINING OXIDANTS AND SPECIAL CARBOXYLIC ACID ESTERS
    申请人:Henkel AG & Co. KGaA
    公开号:US20180140523A1
    公开(公告)日:2018-05-24
    The subject matter of the present disclosure includes agents for lightening keratin fibers, more particularly human hair, containing in a cosmetic carrier: (a) at least one carboxylic acid ester of the formula (I) (b) at least one peroxide compound, and (c) water, wherein the agent has a pH value in the range of from about 7.5 to about 12.5. A further subject matter of the present disclosure includes a kit-of-parts in which the aforementioned components exist packed separately in two agents (A) and (B).
  • US9409905B2
    申请人:——
    公开号:US9409905B2
    公开(公告)日:2016-08-09
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