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2-(hydroxymethyl)-2-(((4-methoxybenzyl)oxy)methyl)propane-1,3-diol | 186090-81-3

中文名称
——
中文别名
——
英文名称
2-(hydroxymethyl)-2-(((4-methoxybenzyl)oxy)methyl)propane-1,3-diol
英文别名
2-(Hydroxymethyl)-2-[(4-methoxyphenyl)methoxymethyl]propane-1,3-diol
2-(hydroxymethyl)-2-(((4-methoxybenzyl)oxy)methyl)propane-1,3-diol化学式
CAS
186090-81-3
化学式
C13H20O5
mdl
——
分子量
256.299
InChiKey
BRIAGXLQRKPEMP-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):
    -0.4
  • 重原子数:
    18
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    79.2
  • 氢给体数:
    3
  • 氢受体数:
    5

上下游信息

  • 下游产品
    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:
    2-(hydroxymethyl)-2-(((4-methoxybenzyl)oxy)methyl)propane-1,3-diol吡啶 、 sodium hydride 作用下, 以 四氢呋喃 、 mineral oil 为溶剂, 反应 18.0h, 生成 3-[(4-methoxybenzyloxy)methyl]-oxetan-3-ylmethanol
    参考文献:
    名称:
    设计和合成新颖的1,25-二羟基维生素D 3类似物,其螺环氧杂环丁烷稠合在A环的C2位置
    摘要:
    设计并合成了四种结构新颖的1,25-二羟基维生素D 3(3a - d)的立体异构体,它们在A环的C2位置稠合了螺-氧杂环丁烷。维生素D类似物(3a,b)和(3c,d)的必需的A环烯炔前体(13a,b)分别根据十一步程序由季戊四醇合成。使用牛胸腺维生素D受体(VDR)对类似物进行的初步生物学评估表明,掺入螺-氧杂环丁烷部分而不是宝石在C 2位的-二甲基对VDR亲和力具有有益的作用。
    DOI:
    10.1016/j.bmc.2013.06.032
  • 作为产物:
    参考文献:
    名称:
    Synthesis of a Nonavalent Mannoside Glycodendrimer Based on Pentaerythritol
    摘要:
    A nonavalent glycodendrimer bearing terminal alpha-D-mannopyranoside units has been synthesized with a convergent approach. Terminal trivalent mannoside dendrons bearing p-halophenyl ethers were prepared by glycosylation of pentaerythritol derivatives having three 2-hydroxyethyl ether substituents. Two efficient routes were developed for the synthesis of the pentaerythritol-based core (17), which has three terminal propargyl ethers. Conditions were found under which the triple Sonogashira coupling reaction of the dendron and the tri-O-propargyl ether (17) proceeded efficiently. The product was deprotected and it and precursors were fully characterized by NMR spectroscopy and FT-ICR mass spectrometry.
    DOI:
    10.1021/jo052045u
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文献信息

  • CATIONIC LIPIDS
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20200331841A1
    公开(公告)日:2020-10-22
    The present invention provides a technique that enables introduction of active ingredients, in particular, nucleic acids, into cells with superior efficiency; and cationic lipids, etc., for use in the technique. The compound or a salt thereof according to the present invention is a compound represented by formula (I) or a salt thereof. In formula (I), n represents an integer of 2 to 5, R represents a linear C 1-5 alkyl group, a linear C 7-11 alkenyl group, or a linear C 11 alkadienyl group, and wavy lines each independently represent a cis-bond or a trans-bond.
    本发明提供了一种技术,能够以优越的效率将活性成分,特别是核酸,引入细胞中;以及用于该技术的阳离子脂质等。根据本发明的化合物或其盐是由式(I)表示的化合物或其盐。在式(I)中,n代表2到5的整数,R代表线性C1-5烷基基团、线性C7-11烯基基团或线性C11烯二烯基团,波浪线各自独立表示顺式键或反式键。
  • Synthesis of New Components for Tethered Bilayer Membranes and Preliminary Surface Characterization.
    作者:Christopher J.Burns、Leslie D. Field、Peter Culshaw、Mohammed Islam、Damon D. Ridley、Jacqueline Morgan、Burkhard Raguse、Lech Wieczorek、Matthew Wilkinson、Valentina Vignevich
    DOI:10.1071/ch99159
    日期:——

    Two analogues of the membrane-forming species PhCH2SS(C24H40O14)(C20H41) (1) have been prepared via short synthetic routes. The compounds readily form self-assembled monolayers on gold. PhCH2SS(C27H45O16)(C20H41)2 PhCH2SS(C29H48O17)(C20H41)3

    已准备好两种模拟膜形成物种PhCH2SS(C24H40O14)(C20H41)(1),通过简短的合成途径。这些化合物容易在表面上形成自组装单分子层。PhCH2SS(C27H45O16)(C20H41)2和PhCH2SS(C29H48O17)(C20H41)3。
  • Self-Assembly of Maltoheptaose-<i>block</i>-polycaprolactone Copolymers: Carbohydrate-Decorated Nanoparticles with Tunable Morphology and Size in Aqueous Media
    作者:Takuya Isono、Kana Miyachi、Yusuke Satoh、Ryosuke Nakamura、Yao Zhang、Issei Otsuka、Kenji Tajima、Toyoji Kakuchi、Redouane Borsali、Toshifumi Satoh
    DOI:10.1021/acs.macromol.6b00781
    日期:2016.6.14
    This paper describes the systematic investigation into the aqueous self-assembly of a series of block copolymers (BCPs) consisting of maltoheptaose (MH; as the A block) and poly(e-caprolactone) (PCL; as the B block), i.e., linear AB-type diblock copolymers with varied PCL molecular weights (MH-b-PC1-(2.5(k,3.3k,5k10k))), AB(y)-type = 2, MH-b(PCL5k) 2; y = 3, MH-b-(PCL3.3k)(3)), A(2)B(2)-type ((MH)(2)-b(PCL(5)k)(2)), and AxB-type miktoarm star polymers (x = 2, (MH)2-b-PCL10k; x = 3, (MH)(3)-b-PCLiok), which had been precisely synthesized via the combination of the living ring opening polymerization and click reaction. Under similar conditions, the nanoprecipitation method was employed to self -assemble them in an aqueous medium. Imaging and dynamic light scattering techniques indicated the successful formation of the carbohydrate -decorated nanoparticles via self -assembly. The MH-b-PCLs formed regular core shell micellar nanoparticles with the hydrodynamic "radius (Rh) of 17-43 nm. MH-b-(PCL5k)2 and MH-b-(PCL3.3k)(3), which have an NPCL comparable to MH-b-PCLiok, were found to form large compound micelles with relatively large radii (Rh of 49 and 56 nm, respectively). On the other hand, (MH),-b-(PCL5k),, (MH),-b-PCLiok, and (MH)3-bPCLiok predominantly formed the regular core shell micellar nanoparticles (Rh = 29-39 nm) with a size smaller than that of MH-b-PCLiok (Rh = 43 nm).
  • Synthesis and application of α-?-mannosyl clusters as photoaffinity ligands for mannose-binding proteins: Concanavalin A as a model receptor
    作者:J Lehmann
    DOI:10.1016/s0008-6215(96)00207-8
    日期:1996.11.20
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