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2-溴丙胺氢溴酸盐 | 2403-33-0

中文名称
2-溴丙胺氢溴酸盐
中文别名
——
英文名称
2-bromopropylamine hydrobromide
英文别名
2-bromo-propylamine; hydrobromide;2-Brom-propylamin; Hydrobromid;bromwasserstoffsaures β-Brom-propylamin;Brom-2-propylamin;2-Bromopropan-1-amine hydrobromide;2-bromopropan-1-amine;hydrobromide
2-溴丙胺氢溴酸盐化学式
CAS
2403-33-0
化学式
BrH*C3H8BrN
mdl
——
分子量
218.919
InChiKey
RELBUBTYJUVMSI-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

物化性质

  • 熔点:
    161-162 °C

计算性质

  • 辛醇/水分配系数(LogP):
    1.31
  • 重原子数:
    6
  • 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:
    26
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2921199090
  • 危险性防范说明:
    P261,P305+P351+P338
  • 危险性描述:
    H302,H315,H319,H335
  • 储存条件:
    存储条件为2-8°C,并需保存在惰性气体环境中。

SDS

SDS:379b47fd66bbcef69bcae86027f2995e
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反应信息

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文献信息

  • Fabrication of mixed-matrix membrane containing metal–organic framework composite with task-specific ionic liquid for efficient CO<sub>2</sub> separation
    作者:Jing Ma、Yunpan Ying、Xiangyu Guo、Hongliang Huang、Dahuan Liu、Chongli Zhong
    DOI:10.1039/c6ta02611g
    日期:——
    fabricate MMMs with different loadings. The prepared TSIL@NH2-MIL-101(Cr)/PIM-1 membrane exhibits largely improved gas permeability and selectivity for CO2/N2 separation, with CO2 permeation values of 2979 Barrer and a CO2/N2 separation selectivity of 37 at 5 wt% loading. Compared with NH2-MIL-101(Cr)/PIM-1 and PIM-1 membranes, the CO2/N2 separation selectivity was increased by 116% and 119%, respectively
    近年来,混合基质膜(MMM)在基于膜的气体分离中显示出优势,但是,仍然强烈要求开发一种设计有效填料的适当方法,以进一步提高MMM的气体分离性能。在这项工作中,提出了通过将特定任务的离子液体(TSIL)加载到金属有机框架(MOF)中来选择性促进CO 2传输的纳米多孔材料。选择[C 3 NH 2 bim] [Tf 2 N]和NH 2 -MIL-101(Cr)作为示范性的TSIL和MOF。含胺的TSIL用作选择性的CO 2转运载体,对改善CO 2可能是有益的渗透率和CO 2 / N 2选择性。同时,NH 2 -MIL-101(Cr)是一种合适的多孔基质材料,可以控制TSIL的良好分散,并可以有效地暴露TSIL的更多活性吸附位。同时,含胺的多孔MOF有助于快速的CO 2输送并进一步提高了CO 2的渗透性。我们进一步将多孔复合材料并入PIM-1中,以制造具有不同负载的MMM。制备的TSIL @ NH
  • 4-[(Cycloalkyl or cycloalkenyl substituted) amino, alkylamino or
    申请人:American Cyanamid Company
    公开号:US04423051A1
    公开(公告)日:1983-12-27
    This disclosure describes novel 4-[(cycloalkyl or cycloalkenyl substituted)amino, alkylamino or alkenylamino]-benzoic acids, salts and derviatives of these such as cycloalkylamino, cycloalkenylamino, cycloalkyl-alkylamino, cycloalkyl-alkenylamino, cycloalkenyl-alkylamino, and cycloalkyl-cycloalkylamino benzoic acids and derivatives and suitable salts of these; these compounds are useful as hypolipidemic and antiatherosclerotic agents.
    本公开说明了新型4-[(环烷基或环烯基取代)氨基、烷基氨基或烯基氨基]-苯甲酸,以及这些化合物的盐和衍生物,例如环烷基氨基、环烯基氨基、环烷基-烷基氨基、环烷基-烯基氨基、环烯基-烷基氨基和环烷基-环烷基氨基苯甲酸和衍生物,以及这些化合物的适当盐;这些化合物可用作降脂和抗动脉粥样硬化药物。
  • 4-[(Cycloalkyl or cycloalkenyl substituted)amino, alkylamino or
    申请人:American Cyanamid Company
    公开号:US04227014A1
    公开(公告)日:1980-10-07
    This disclosure describes novel 4-[(cycloalkyl or cycloalkenyl substituted)amino, alkylamino or alkenylamino]-benzoic acids, salts and derivatives of these such as cycloalkylamino, cycloalkenylamino, cycloalkyl-alkylamino, cycloalkylalkenylamino, cycloalkenyl-alkylamino, and cycloalkyl-cycloalkylamino benzoic acids and derivatives and suitable salts of these; these compounds are useful as hypolipidemic and antiatherosclerotic agents.
    本披露描述了新型的4-[(环烷基或环烯基取代)氨基,烷基氨基或烯基氨基]-苯甲酸,以及这些化合物的盐和衍生物,例如环烷基氨基,环烯基氨基,环烷基-烷基氨基,环烷基烯基氨基,环烯基-烷基氨基和环烷基-环烷基氨基苯甲酸及其衍生物和合适的盐。这些化合物可用作降血脂和抗动脉粥样硬化药物。
  • Method of treating hyperlipidemia with 4-(monoalkylamino)benzoic acid
    申请人:American Cyanamid Company
    公开号:US04485105A1
    公开(公告)日:1984-11-27
    This disclosure describes a method of treating hyperlipidemia and atherosclerotic lesions with 4-(monoalkylamino)benzoic acid amides and compositions therefor.
    本披露描述了使用4-(单烷基氨基)苯甲酸酰胺及其组合物治疗高脂血症和动脉粥样硬化病变的方法。
  • Sulfonamide herbicide antidote compositions and method of use
    申请人:Stauffer Chemical Company
    公开号:US04021229A1
    公开(公告)日:1977-05-03
    Herbicidal compositions consisting of an active herbicidal compound and an antidote therefor and the methods of use of the herbicide compositions are described herein. The antidote compound corresponds to the formula ##STR1## wherein R.sub.1 can be selected from the group consisting of alkyl, haloalkyl, halogen, isocyanate, alkenylamino, halophenylamino, phenyl, substituted phenyl wherein said substituents can be selected from alkyl, alkoxy, halogen, nitro, amino and haloalkylaminosulfonyl; R.sub.2 and R.sub.3 can be the same or different and can be selected from hydrogen, alkyl, haloalkyl, alkoxy, alkenyl, alkynyl, alkynoxy, haloalkoxycarbonyl, alkynoxycarbonyl, carbamoyl, haloalkylthio, diacetonitrilocarbamyl, phenyl, substituted phenyl wherein said substituents can be selected from alkoxy, halogen, hydroxy, nitro and carbamoyl, and R.sub.2 and R.sub.3 taken together form the ring structure alkyloxazolidyl.
    本文描述了由活性除草剂化合物和其解毒剂组成的除草剂组合物及其使用方法。解毒剂化合物对应于公式##STR1##其中R.sub.1可以从包括烷基,卤代烷基,卤素,异氰酸酯,烯基氨基,卤代苯基氨基,苯基,取代苯基(其中所述取代基可以从烷基,烷氧基,卤素,硝基,氨基和卤代烷基氨基磺酰中选择)中选择;R.sub.2和R.sub.3可以相同或不同,并且可以从氢,烷基,卤代烷基,烷氧基,烯基,炔基,炔氧基羰基,炔氧羰基,氨基甲酰,卤代烷基硫,二乙腈基氨基甲酰,苯基,取代苯基(其中所述取代基可以从烷氧基,卤素,羟基,硝基和氨甲酰中选择),并且R.sub.2和R.sub.3在一起形成环状结构烷氧噁唑基。
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