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2-amino-N,N-2-trimethylpropane-1-sulfonamide | 1037833-08-1

中文名称
——
中文别名
——
英文名称
2-amino-N,N-2-trimethylpropane-1-sulfonamide
英文别名
2-amino-N,N,2-trimethylpropane-1-sulfonamide
2-amino-N,N-2-trimethylpropane-1-sulfonamide化学式
CAS
1037833-08-1
化学式
C6H16N2O2S
mdl
——
分子量
180.271
InChiKey
UIJBSCXSHNAYLB-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):
    -0.8
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    71.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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:
    参考文献:
    名称:
    N,N-Dichloroaminosulfonic acids as novel topical antimicrobial agents
    摘要:
    2-Dichloroamino-2-methyl-propane-1-sulfonic acid sodium salt (2a), a stable derivative of endogenous N,N-dichlorotaurine (1), has been identified and is under development as a topical antimicrobial agent. Structure-activity relationships of analogs were explored to achieve optimal antimicrobial activity with minimal mammalian toxicity while maintaining the desired stability. All the analogs synthesized showed antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Candida albicans in the range of 1-128 mu g/mL and cytotoxicity against mammalian L929 cells in the range 80-1900 mu g/mL. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.10.114
  • 作为产物:
    描述:
    benzyl 1-(N,N-dimethylsulfamoyl)-2-methylpropan-2-ylcarbamate 在 palladium 10% on activated carbon 氢气 作用下, 以 甲醇 为溶剂, 反应 17.08h, 以91%的产率得到2-amino-N,N-2-trimethylpropane-1-sulfonamide
    参考文献:
    名称:
    WO2008/83347
    摘要:
    公开号:
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文献信息

  • WO2008/83347
    申请人:——
    公开号:——
    公开(公告)日:——
  • N-HALOGENATED AMINO COMPOUNDS AND DERIVATIVES
    申请人:NovaBay Pharmaceuticals, Inc.
    公开号:EP2120965B1
    公开(公告)日:2014-11-05
  • US8415497B2
    申请人:——
    公开号:US8415497B2
    公开(公告)日:2013-04-09
  • [EN] N-HALOGENATED AMINO COMPOUNDS AND DERIVATIVES<br/>[FR] COMPOSÉS AMINÉS HALOGÉNÉS EN N ET DÉRIVÉS DE CEUX-CI
    申请人:NOVABAY PHARMACEUTICALS INC
    公开号:WO2008083347A1
    公开(公告)日:2008-07-10
    [EN] The present invention relates to active bactericidal, antibacterial, anti-infective, antimicrobial, sporicidal, disinfectant, antifungal and antiviral compounds and compositions and to new uses of these compositions in therapy. This specification also describes methods of use for the new compounds and compositions. The specification further describes methods for preparing these compounds.
    [FR] La présente invention concerne des composés actifs bactéricides, antibactériens, anti-infectieux, antimicrobiens, sporicides, désinfectants, antifongiques et antiviraux, des compositions et de nouvelles utilisations de ces compositions en thérapie. La présente invention concerne également des procédés d'utilisation pour les nouveaux composés et compositions. L'invention concerne en outre des procédés servant à préparer ces composés.
  • N,N-Dichloroaminosulfonic acids as novel topical antimicrobial agents
    作者:Eddy Low、Satheesh Nair、Timothy Shiau、Barbara Belisle、Dmitri Debabov、Chris Celeri、Meghan Zuck、Ron Najafi、Nafsika Georgopapadakou、Rakesh Jain
    DOI:10.1016/j.bmcl.2008.10.114
    日期:2009.1
    2-Dichloroamino-2-methyl-propane-1-sulfonic acid sodium salt (2a), a stable derivative of endogenous N,N-dichlorotaurine (1), has been identified and is under development as a topical antimicrobial agent. Structure-activity relationships of analogs were explored to achieve optimal antimicrobial activity with minimal mammalian toxicity while maintaining the desired stability. All the analogs synthesized showed antimicrobial activity against Staphylococcus aureus, Escherichia coli, and Candida albicans in the range of 1-128 mu g/mL and cytotoxicity against mammalian L929 cells in the range 80-1900 mu g/mL. (C) 2008 Elsevier Ltd. All rights reserved.
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