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羟胺-甲基三乙二醇 | 248275-10-7

中文名称
羟胺-甲基三乙二醇
中文别名
——
英文名称
O-(2-(2-(2-methoxyethoxy)ethoxy)ethyl)hydroxylamine
英文别名
Aminooxy-PEG3-methane;O-[2-[2-(2-methoxyethoxy)ethoxy]ethyl]hydroxylamine
羟胺-甲基三乙二醇化学式
CAS
248275-10-7
化学式
C7H17NO4
mdl
——
分子量
179.216
InChiKey
UPZRLQLRXOQKOM-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):
    -1.1
  • 重原子数:
    12
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    62.9
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • WATER-SOLUBLE ZINC IONOPHORES, ZINC CHELATORS, AND/OR ZINC COMPLEXES AND USE FOR TREATING CANCER
    申请人:Magda Darren
    公开号:US20070219276A1
    公开(公告)日:2007-09-20
    Disclosed herein are novel zinc ionophores, zinc chelators and/or zinc complexes with enhanced aqueous solubility. Methods of treating cancer using at least one zinc ionophore and/or zinc chelator are also disclosed. Also disclosed herein are compositions and methods for treating cancer with combination therapy using at least one texaphyrin metal complex and at least one zinc ionophore or the respective pharmaceutically acceptable derivatives or salts thereof.
    本文披露了新型锌离子载体、锌螯合剂和/或具有增强水溶性的锌络合物。还披露了使用至少一种锌离子载体和/或锌螯合剂治疗癌症的方法。本文还披露了使用至少一种锌离子载体或其相应的药用可接受衍生物或盐与至少一种锌离子载体或其相应的药用可接受衍生物或盐的联合疗法来治疗癌症的组合疗法的组合物和方法。
  • [EN] NOVEL CYANOGUANIDINES<br/>[FR] NOUVELLES CYANOGUANIDINES
    申请人:TOPOTARGET AS
    公开号:WO2009086835A1
    公开(公告)日:2009-07-16
    This application discloses novel cyanoguanidines of the formula (I) wherein A is selected from -C(=O)-, -S(=O)2-, -C(=S)-, and -P(=O)(R5)-, wherein R5 is selected from C1-6-alkyl, C1-6-alkoxy, and hydroxy; B is selected from a single bond, -O-, -NR6- and -C(=O)-NR6-, wherein R6 is selected from hydrogen, optionally substituted C1-12-alkyl, optionally substituted C1-12-alkenyl, optionally substituted aryl, optionally substituted heterocyclyl, and optionally substituted heteroaryl; and m is an integer of 0-12 and n is an integer of 0-12, wherein the sum m+n is 1-20; and R1 is selected from optionally substituted heteroaryl; and pharmaceutically acceptable salts thereof, and prodrugs thereof. The compounds are usefuld for use as a medicament for the treatment of a disease or a condition caused by an elevated level of nicotinamide phosphoribosyltransferase (NAMPRT).
    该申请公开了一种新型氰胍啶化合物,其化学式为(I),其中A从-C(=O)-,-S(=O)2-,-C(=S)-和-P(=O)(R5)-中选择,其中R5选择自C1-6-烷基,C1-6-烷氧基和羟基;B从单键,-O-,-NR6-和-C(=O)-NR6-中选择,其中R6选择自氢,可选择地取代的C1-12-烷基,可选择地取代的C1-12-烯基,可选择地取代的芳基,可选择地取代的杂环烷基和可选择地取代的杂环芳基;m为0-12的整数,n为0-12的整数,其中m+n之和为1-20;R1选择自可选择地取代的杂环芳基;以及其药学上可接受的盐和前药。这些化合物可用作治疗由烟酰胺磷酸核糖转移酶(NAMPRT)水平升高引起的疾病或病况的药物。
  • CONTROLLED RELEASE OF ACTIVE COMPOUNDS FROM DYNAMIC MIXTURES
    申请人:Herrmann Andreas
    公开号:US20100226875A1
    公开(公告)日:2010-09-09
    The present invention relates to a dynamic mixture in the form of a dynamic mixture obtained by reacting together, in the presence of water, at least one O-substituted hydroxylamine or S-substituted thiohydroxylamine derivative with at least one perfuming, flavoring, insect repellent or attractant, bactericide or fungicide aldehyde or ketone. This mixture is capable of releasing in a controlled and prolonged manner the aldehyde or ketone into the surrounding environment. Furthermore, the present invention concerns also the use of these dynamic mixtures as perfuming ingredients as well as the perfuming compositions or perfumed articles that include these mixtures.
    本发明涉及一种动态混合物,其为通过在水的存在下将至少一种O-取代羟胺或S-取代硫羟胺衍生物与至少一种香料、调味剂、驱虫剂或诱引剂、杀菌剂或杀真菌剂醛或酮反应而得到的动态混合物。该混合物能够以受控和延长的方式释放醛或酮进入周围环境。此外,本发明还涉及将这些动态混合物用作调香成分以及包括这些混合物的调香组合物或香气物品的用途。
  • ORGANIC COMPOUNDS
    申请人:Resene Paints Limited
    公开号:US20140331895A1
    公开(公告)日:2014-11-13
    The present invention relates to cellulose mixed esters, processes for preparing these and uses of the cellulose mixed esters, for example in coating compositions. The cellulose mixed esters have glass transition temperatures that fall within an appropriate range to allow for film formation to occur at ambient temperatures and have a total degree of substitution per anhydroglucose unit of about 2.5 to about 3.5; a residual hydroxyl functionality per anhydroglucose unit of 0 to about 0.5; a degree of substitution per anhydroglucose unit by C 2 -C 6 ester groups of about 0.5 to about 2.8; and a degree of substitution per anhydroglucose unit by Ievulinyl ester groups of about 0.2 to about 2.6.
    本发明涉及纤维素混合酯、制备这些酯的方法以及纤维素混合酯的用途,例如在涂料组合物中的用途。纤维素混合酯具有适当范围内的玻璃转移温度,使得在常温下可以进行薄膜形成,并且每个无水葡萄糖单元的总取代度约为2.5至3.5;每个无水葡萄糖单元的剩余羟基功能为0至0.5;每个无水葡萄糖单元的C2-C6酯基的取代度约为0.5至2.8;每个无水葡萄糖单元的丙酮酸乙酯酯基的取代度约为0.2至2.6。
  • Derivatives of 6-(2,3-dichlorophenyl)-1,2,4-triazin-5-amine
    申请人:Nektar Therapeutics
    公开号:US10189859B2
    公开(公告)日:2019-01-29
    The instant disclosure relates to (among other things) compounds that are derivatives of 6-(2,3-dichlorophenyl)-1,2,4-triazin-5-amine. The compounds provided possess unique effects and differences over other phenyltriazines known in the art.
    本公开涉及 6-(2,3-二氯苯基)-1,2,4-三嗪-5-胺衍生物的化合物。与本领域已知的其他苯基三嗪相比,所提供的化合物具有独特的效果和差异。
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