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2-(三甲基甲硅烷基)乙胺盐酸盐 | 18135-30-3

中文名称
2-(三甲基甲硅烷基)乙胺盐酸盐
中文别名
2-(三甲基硅基)乙胺基盐酸盐
英文名称
2-(trimethylsilyl)-ethylamine hydrochloride
英文别名
2-trimethylsilanyl-ethylamine hydrochloride;2-(trimethylsilyl)ethan-1-amine hydrochloride;(2-aminoethyl)trimethylsilane hydrochloride;{me3Si(et-2-NH3)}Cl;2-Trimethylsilyl-aethylamin; Hydrochlorid;trimethylsilylethylamine hydrochloride;TMSCH2CH2NH2*HCl;2-Trimethylsilylethylazanium;chloride;2-trimethylsilylethylazanium;chloride
2-(三甲基甲硅烷基)乙胺盐酸盐化学式
CAS
18135-30-3
化学式
C5H16NSi*Cl
mdl
MFCD12545815
分子量
153.727
InChiKey
OECFYIVZLPNYAX-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):
    1.23
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    26
  • 氢给体数:
    2
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2-(三甲基甲硅烷基)乙胺盐酸盐N,N-二异丙基乙胺 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 反应 16.0h, 生成 4-Chloro-2-(methylamino)-6-(2-(trimethylsilyl)ethylamino)pyrimidine-5-carbaldehyde
    参考文献:
    名称:
    Synthesis of a β-glycoside functionalized GΛC motif for self-assembly into rosette nanotubes with predefined length
    摘要:
    Progress toward the synthesis of guanine cytosine (G Lambda C) oligonucleotides for the spontaneous self-assembly of rosette nanotubes (RNTs) with predefined length is described. Highlighted is the synthesis of the beta-glycoside functionalized G Lambda C base along with a new nitrogen protecting group strategy that is compatible with Boc and Bn groups. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2010.11.122
  • 作为产物:
    描述:
    N-<2-(trimethylsilyl)ethyl>phthalimide一水合肼盐酸 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以860 mg的产率得到2-(三甲基甲硅烷基)乙胺盐酸盐
    参考文献:
    名称:
    一种抑制激酶化合物及其在医学上的用途
    摘要:
    一种抑制激酶化合物及其在医学上的用途。本发明提供式(I)化合物,其立体异构体、互变异构体或药学上可接受的盐,其作为FGFR4激酶选择性抑制剂及其在制备治疗由FGFR4或FGF19所致疾病的药物或药物组合物中的应用,本发明公开的化合物对FGFR4具有选择性的显著抑制活性,在肿瘤治疗领域具有广泛的应用前景。
    公开号:
    CN108341837A
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文献信息

  • [EN] PYRROLIDINE DERIVATIVES AND THEIR USE AS COMPLEMENT PATHWAY MODULATORS<br/>[FR] DÉRIVÉS PYRROLIDINE ET LEUR UTILISATION EN TANT QUE MODULATEURS DE LA VOIE DU COMPLÉMENT
    申请人:NOVARTIS AG
    公开号:WO2014002053A1
    公开(公告)日:2014-01-03
    The present invention provides a compound of formula (I) a method for manufacturing the compounds of the invention and its therapeutic uses as complement pathway modulators for the treatment of ocular diseases. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.
    本发明提供了一种化合物(I)的方法,用于制造该发明的化合物以及其作为眼部疾病治疗的补体途径调节剂的治疗用途。本发明还提供了一种药理活性剂的组合和一种药物组合物。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Si: MVol.C, 93, page 253 - 257
    作者:
    DOI:——
    日期:——
  • Repurposing of a drug scaffold: Identification of novel sila analogues of rimonabant as potent antitubercular agents
    作者:Remya Ramesh、Rahul D. Shingare、Vinod Kumar、Amitesh Anand、Swetha B、Sridhar Veeraraghavan、Srikant Viswanadha、Ramesh Ummanni、Rajesh Gokhale、D. Srinivasa Reddy
    DOI:10.1016/j.ejmech.2016.07.009
    日期:2016.10
    The structural similarity between an MmpL3 inhibitor BM212, and a cannabinoid receptor modulator rimonabant, prompted us to investigate the anti-tubercular activity of rimonabant and its analogues. Further optimization, particularly through incorporation of silicon into the scaffold, resulted in new compounds with significant improvement in anti-tubercular activity against Mycobacterium tuberculosis (H37Rv). The sila analogue 18a was found to be the most potent antimycobacterial compound (MIC, 31 ng/mL) from this series with an excellent selectivity index. (C) 2016 Elsevier Masson SAS. All rights reserved.
  • Aliphatic Organo-functional Siloxanes<sup>1</sup>
    作者:L. H. Sommer、R. P. Pioch、N. S. Marans、G. M. Goldberg、J. Rockett、J. Kerlin
    DOI:10.1021/ja01108a042
    日期:1953.6
  • NOVEL HETEROARYL-UREA COMPOUNDS AS KV7.2 INHIBITORS
    申请人:[en]ICAGEN, LLC
    公开号:WO2023091554A1
    公开(公告)日:2023-05-25
    The invention provides new heteroaromatic compounds having the general formula (I'), or a solvate or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5, R6, Y1, Y2, Y3, and n are as defined herein, compositions including the compounds, processes of manufacturing the compounds and methods of using the compounds.
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