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7-amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole sulfuric acid salt | 689293-72-9

中文名称
——
中文别名
——
英文名称
7-amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole sulfuric acid salt
英文别名
7-amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole hydrosulfate;2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-amine sulfate;2,3-dihydro-1H-imidazo[1,2-b]pyrazol-7-amine;sulfuric acid
7-amino-2,3-dihydro-1H-imidazo[1,2-b]pyrazole sulfuric acid salt化学式
CAS
689293-72-9
化学式
C5H8N4*H2O4S
mdl
——
分子量
222.225
InChiKey
CYUSVPRYCYBUJZ-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):
    -0.76
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    139
  • 氢给体数:
    4
  • 氢受体数:
    7

反应信息

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文献信息

  • Hair dye containing aminopyrazole derivatives as well as pyrazole
    申请人:Wella Aktiengesellschaft
    公开号:US05380340A1
    公开(公告)日:1995-01-10
    The composition for oxidative dyeing of hair contains at least one coupler and 0.010 to 3.0 percent by weight of at least one developer selected from the group consisting of aminopyrazole derivatives of the formula (I): ##STR1## wherein R is selected from the group consisting of hydrogen and alkyl groups having one to four carbon atoms; n=2 or 3; and physiologically tolerated, water-soluble salts thereof. The developer and coupler substances are present in the composition in a total amount of from 0.1 to 5.0 percent. New pyrazole derivative compounds are also part of the invention.
    染发氧化染料的组成物至少包含一种偶联剂和0.010至3.0重量百分比的至少一种选择自吡唑生物的开发剂,其化学式为(I):其中R选择自氢和碳原子数为1至4的烷基基团的群;n=2或3;以及其生理耐受的溶性盐。开发剂和偶联剂物质在组成物中的总量为0.1至5.0百分比。新的吡唑生物化合物也属于该发明的一部分。
  • Cephem compounds
    申请人:Fujisawa Pharmaceutical Co., Ltd
    公开号:US20040132994A1
    公开(公告)日:2004-07-08
    The present invention relates to a compound of the formula [I]: 1 wherein R 1 is lower alkyl, hydroxy(lower)alkyl or halo(lower)alkyl, and R 2 is hydrogen or amino protecting group, or R 1 and R 2 are bonded together and form lower alkylene or lower alkenylene; R 3 is hydrogen or lower alkyl; R 4 is 2 R 5 is carboxy or protected carboxy; and R 6 is amino or protected amino, or a pharmaceutically acceptable salt thereof, a process for preparing a compound of the formula [I], and a pharmaceutical composition comprising a compound of the formula [I] in admixture with a pharmaceutically acceptable carrier.
    本发明涉及一种化合物,其分子式为[I]:1其中R1是低级烷基,羟基(低级)烷基或卤代(低级)烷基,而R2是氢或基保护基,或R1和R2相互结合形成低级亚烷基或低级烯基亚烷基;R3是氢或低级烷基;R4是2;R5是羧基或保护羧基;而R6是基或保护基,或其药学上可接受的盐,一种制备分子式[I]化合物的方法,以及包含分子式[I]化合物与药学上可接受的载体混合的制药组合物。
  • Cephem Compounds and Use as Antimicrobial Agents
    申请人:Yamanaka Toshio
    公开号:US20090012054A1
    公开(公告)日:2009-01-08
    The present invention provides a compound of the formula [I]: wherein R1 is lower alkyl, etc. and R2 is hydrogen, etc., or R1 and R2 are bonded together to form lower alkylene; R3 is a group represented by wherein R6 and R7 are independently optionally protected amino, etc.; m and n are independently an integer of 0 to 6; R8 and R9 are independently optionally protected amino, etc., and q and r are independently an integer of 0 to 6, or R8 and R9, together with the adjacent alkylene(s) and the nitrogen atom, form saturated nitrogen-containing heterocycle optionally having substituent(s); R4 is lower alkyl, etc.; and R5 is amino, etc., or a pharmaceutically acceptable salt thereof.
    本发明提供了一种化合物,其化学式为[I]:其中R1是低碳基等,R2是氢等,或者R1和R2结合形成低碳基烯;R3是一个由表示的基团,其中R6和R7分别是可选的保护基等;m和n分别是0到6的整数;R8和R9分别是可选的保护基等,q和r分别是0到6的整数,或者R8和R9与相邻的烷基和氮原子结合形成饱和的含氮杂环,该杂环可以有取代基;R4是低碳基等;R5是基等,或其药学上可接受的盐。
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