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potassium N-methylsulfamate | 84077-80-5

中文名称
——
中文别名
——
英文名称
potassium N-methylsulfamate
英文别名
potassium methylsulfamate;N-methylsulfamic acid potassium salt;potassium;N-methylsulfamate
potassium N-methylsulfamate化学式
CAS
84077-80-5
化学式
CH4NO3S*K
mdl
——
分子量
149.212
InChiKey
ZRXCPOMDITWQIF-UHFFFAOYSA-M
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):
    -4.33
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    缩水甘油potassium N-methylsulfamate 为溶剂, 反应 12.0h, 以90%的产率得到potassium N-(1,2-dihydroxypropyl)-N-methylamidosulfonate
    参考文献:
    名称:
    氨基磺酸衍生物与环氧化物的反应
    摘要:
    氨基磺酸和N-烷基氨基磺酸的盐与缩水甘油、表氯醇和环氧醚反应得到相应的官能取代的β-羟基烷基氨基磺酸盐。
    DOI:
    10.1007/bf01558065
  • 作为产物:
    描述:
    甲氨基磺酸氢氧化钾 以97%的产率得到
    参考文献:
    名称:
    GAER, S. A.;GAREEV, G. A.;STEPANOVA, N. V.;SAKOVICH, G. V.;BOLSHEDVORSKAY+, ZH. OBSHCH. XIMII, 60,(1990) N, S. 1490-1496
    摘要:
    DOI:
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文献信息

  • The reaction of sulfamic acid derivatives with epoxides
    作者:A. S. Ermakov、P. V. Bulatov、V. A. Tartakovsky
    DOI:10.1007/bf02495401
    日期:1997.3
    Reactions of diglycidyl and allylglycidyl ethers with salts of sulfamic acid followed by acidic hydrolysis of the products afforded the corresponding aminoethers. The alcoholysis of sulfamic acids with ethanol was suggested as a method for mild elimination of the sulfo group.
    二缩水甘油醚和烯丙基缩水甘油醚与氨基磺酸盐的反应,然后产物的酸水解得到相应的氨基醚。氨基磺酸与乙醇的醇解被建议作为温和消除磺基的方法。
  • Synthesis ofN,N′-dialkylmethylenebis(nitramines) fromN-alkylsulfamates
    作者:V. A. Tartakovsky、A. S. Ermakov、N. V. Sigai、O. N. Varfolomeeva
    DOI:10.1007/bf02494897
    日期:2000.6
    Symmetrical and unsymmetricalN,N′-dialkylmethylenebis(nitramines) were obtained fromN-alkylsulfamates by condensation with formaldehyde and subsequent nitration.
    通过与甲醛缩合和随后的硝化从N-烷基氨基磺酸盐获得对称和不对称N,N'-二烷基亚甲基双(硝胺)。
  • New Synthetic Approaches to Functionally Substituted 4,5-Dihydro-1,2,3-oxadiazole 2-Oxides
    作者:V. A. Tartakovskii、A. S. Ermakov、Yu. A. Strelenko、D. B. Vinogradov、E. Yu. Petrov
    DOI:10.1007/s11178-005-0132-z
    日期:2005.1
    A practical procedure has been proposed for the synthesis of functionally substituted 4,5-dihydro-1,2,3-oxadiazole 2-oxides on the basis ofsulfamic acid derivatives.
    提出了一种基于氨基磺酸衍生物合成功能取代的4,5-二氢-1,2,3-恶二唑2-氧化物的实用方法。
  • Process for bleaching keratin fibers
    申请人:Javet Manuela
    公开号:US20070231283A1
    公开(公告)日:2007-10-04
    The present patent application relates to a process for bleaching keratin fibers which is characterized by applying to the fiber a ready-to-use agent having a basic pH and containing: a) at least one bleach booster according to the general formula (I) wherein R1 is a hydrogen, R2 is hydrogen, a substituted or unsubstituted C1- to C12-alkyl group, a substituted or unsubstituted C1- to C12-monohydroxy-alkyl group, a substituted or unsubstituted C2- to C12-polyhydroxy alkyl group, or a substituted saturated, unsaturated or aromatic 4- to 8-membered carbocycle or heterocycle, and R3 is a OR-Group, with R being equal to hydrogen, an ammonium group, or an alkali metal, or an earth alkali metal atom; b) at least one appropriate type-2 bleach-stable direct dye; and c) at least one oxidant, and after an exposure time of 5 to 60 minutes at a temperature of 10 to 70° C. rinsing the fiber with water as well as the use of special type-2 bleach-stable direct dyes for acquiring a natural looking bleaching of keratin fibers, particularly human hair, without undesired undertones.
    本专利申请涉及一种漂白角蛋白纤维的方法,其特征在于将具有碱性pH值的即用型剂涂覆于纤维上,该剂含有:a)至少一种漂白增强剂,其一般式为(I),其中R1为氢,R2为氢、取代或未取代的C1-C12烷基、取代或未取代的C1-C12单羟基烷基、取代或未取代的C2-C12多羟基烷基或取代的饱和、不饱和或芳香4-8成员碳环或杂环,R3为OR-基团,其中R等于氢、铵基或碱金属或碱土金属原子;b)至少一种适当的2型漂白稳定直接染料;以及c)至少一种氧化剂,经过5至60分钟的暴露时间,在10至70℃的温度下,用水冲洗纤维,以及使用特殊的2型漂白稳定直接染料,以获得天然外观的角蛋白纤维漂白,特别是人类头发,无不良底色。
  • Synthesis of β-nitramino derivatives ofgem-dinitroalkanes
    作者:V. A. Tartakovsky、A. S. Ermakov、O. N. Varfolomeeva
    DOI:10.1007/bf02495312
    日期:1999.7
    A method for the synthesis of beta-nitramino derivatives of gem-dinitroalkanes by nitration of the products of condensation of sulfamic acid derivatives with the corresponding gem-dinitroalkanes was proposed.
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