β-(Methylamino)-ethylallylether | 104678-16-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: β-(Methylamino)-ethylallylether
• 英文别名: N-methyl 2-aminoethanol O-allyl ether；(2-allyloxy-ethyl)-methyl-amine；N-methyl-2-prop-2-enoxyethanamine
• CAS: 104678-16-2
• 化学式: C₆H₁₃NO
• 分子量: 115.175
• InChiKey: KYSOMVASXGZGSI-UHFFFAOYSA-N

物化性质

• 沸点：
  132.3±15.0 °C(Predicted)
• 密度：
  0.835±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  8
• 可旋转键数：
  5
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  21.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  β-(Methylamino)-ethylallylether 、 六甲基二硅氮烷 在 糖精 作用下， 生成
  参考文献：
  名称：

  Ugi amine-derived P,N- and P,P-ligands with N-alkyltriethoxysilyl tethers: synthesis and evaluation of mesoporous silica-supported Pd complexes in asymmetric allylic substitution reactions

  摘要：

  A facile approach to the synthesis of several types of chiral P,N- and P,P-ligands bearing triethoxysilyl groups starting from N,N-diemthyl-1-ferrocenylethylamine (Ugi amine) has been developed. Allyl palladium complexes of these ligands have been prepared, characterized, and grafted on mesoporous silica. The resulting silica-supported complexes have been shown to catalyze asymmetric allylic alkylation and aminations reactions with moderate enantioselectivities. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.01.025
• 作为产物：
  描述：

  N-methyl-N-Boc-aminoethanol O-allyl ether 在 硫酸 作用下， 以 二氯甲烷 为溶剂， 以60%的产率得到β-(Methylamino)-ethylallylether
  参考文献：
  名称：

  Ugi amine-derived P,N- and P,P-ligands with N-alkyltriethoxysilyl tethers: synthesis and evaluation of mesoporous silica-supported Pd complexes in asymmetric allylic substitution reactions

  摘要：

  A facile approach to the synthesis of several types of chiral P,N- and P,P-ligands bearing triethoxysilyl groups starting from N,N-diemthyl-1-ferrocenylethylamine (Ugi amine) has been developed. Allyl palladium complexes of these ligands have been prepared, characterized, and grafted on mesoporous silica. The resulting silica-supported complexes have been shown to catalyze asymmetric allylic alkylation and aminations reactions with moderate enantioselectivities. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.01.025

文献信息

• SUBSTITUTED THIOPHENYL URACILS, SALTS THEREOF AND THE USE THEREOF AS HERBICIDAL AGENTS
  申请人：Syngenta Crop Protection AG

  公开号：US20200315174A1

  公开（公告）日：2020-10-08

  The invention relates to substituted thiophenyl uracils of general formula (I) or the salts (I) thereof, wherein the groups in general formula (I) are as defined in the description, and to the use thereof as herbicides, in particular for controlling weeds and/or weed grasses in crops of cultivated plants and/or as plant growth regulators for influencing the growth of crops of cultivated plants.

  本发明涉及取代噻吩基尿嘧啶的通式(I)或其盐(I)，其中通式(I)中的基团如描述中定义，以及作为除草剂，特别是用于控制作物中的杂草和/或杂草草本的用途，以及作为植物生长调节剂用于影响栽培植物作物的生长。
• A Catalytic Oxidative Quinone Heterofunctionalization Method: Synthesis of Strongylophorine-26
  作者：Wanwan Yu、Per Hjerrild、Kristian M. Jacobsen、Henriette N. Tobiesen、Line Clemmensen、Thomas B. Poulsen

  DOI：10.1002/anie.201805580

  日期：2018.7.26

  functionalization with a collection of O, N, and S nucleophiles, using oxygen as the terminal oxidant. Preliminary mechanistic observations and the first synthesis of the cytotoxic natural product strongylophorine‐26 is presented.

  理想情况下，杂原子取代的对苯醌的制备是通过直接添加亲核试剂，然后进行原位再氧化来完成的。尽管是一种引人注目的策略，但对p-醌部分的反应性不容易驯服，也没有广泛适用的杂原子官能化方法。这里示出的是，钴（OAC）2和Mn（OAc）3 ⋅2ħ 2 ö充当强大催化剂氧化p为O，N的集合-quinone官能化，和S的亲核试剂，使用氧作为氧化剂终端。介绍了初步的机械观察结果和细胞毒性天然产物Strongylophorine-26的首次合成。
• Spiroimidazolone derivative
  申请人：Esaki Toru

  公开号：US09169254B2

  公开（公告）日：2015-10-27

  The present invention relates to a compound represented by the following formula (1): wherein W, X, Y, R1, R2, R33, R34, m and n are as defined in the claims, or a pharmacologically acceptable salt thereof.

  本发明涉及一种由以下式(1)表示的化合物：其中W、X、Y、R1、R2、R33、R34、m和n如权利要求中所定义，或其药学上可接受的盐。
• CELL ADHESIVE MATERIAL FOR BIOLOGICAL TISSUE
  申请人：Sanyo Chemical Industries, Ltd.

  公开号：EP2636415A1

  公开（公告）日：2013-09-11

  An object of the present invention is to provide a cell-adhesive material for biological tissues, in which the surface of a material for biological tissues (particularly metallic material) is modified strongly with a large amount of a cell-adhesive artificial peptide (P) that retains a biological activity. The present invention provides a cell-adhesive material for biological tissues including a cell-adhesive artificial peptide (P) and a material for biological tissues, wherein the cell-adhesive artificial peptide (P) is immobilized on the surface of the material for biological tissues through an electrochemical reaction. The cell-adhesive artificial peptide (P) is preferably a peptide (P1) that is synthesized by a genetic recombinant microorganism and has at least one cell-adhesive minimal amino acid sequence (X) in one molecule. The number of the cell-adhesive minimal amino acid sequences (X) in one molecule of the polypeptide (P1) is preferably 3 to 50.

  本发明的目的是提供一种用于生物组织的细胞粘附材料，其中生物组织材料（特别是金属材料）的表面被大量保持生物活性的细胞粘附人工肽（P）强烈修饰。 本发明提供了一种生物组织细胞粘附材料，包括细胞粘附人工肽（P）和生物组织材料，其中细胞粘附人工肽（P）通过电化学反应固定在生物组织材料表面。细胞粘附性人工多肽（P）最好是由基因重组微生物合成的多肽（P1），在一个分子中至少有一个细胞粘附性最小氨基酸序列（X）。在多肽（P1）的一个分子中，细胞粘附性最小氨基酸序列（X）的数量最好为 3 至 50 个。
• PREPARATION METHOD FOR BENZOXAZOLEOXAZINE KETONE COMPOUND AND INTERMEDIATE AND CRYSTAL FORM THEREOF
  申请人：North China Pharmaceutical New Drug R&D Co., Ltd.

  公开号：EP3199536A1

  公开（公告）日：2017-08-02

  A preparation method for a high-purity benzoxazoleoxazine ketone compound, a crystal form thereof, and an intermediate compound for preparing a compound of formula (I), and a preparation method therefor.

  一种高纯度苯并恶唑恶嗪酮化合物、其晶型和制备式（I）化合物的中间体化合物的制备方法及其制备方法。