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1-甲基环丙烷羧酰胺盐酸盐 | 78104-89-9

中文名称
1-甲基环丙烷羧酰胺盐酸盐
中文别名
——
英文名称
1-methylcyclopropanecarboximidamide hydrochloride
英文别名
imino(1-methylcyclopropyl)methanaminium chloride;1-methylcyclopropanecarboximidamide, monohydrochloride;1-Methylcyclopropanecarboxamidine hydrochloride;[Amino-(1-methylcyclopropyl)methylidene]azanium;chloride;[amino-(1-methylcyclopropyl)methylidene]azanium;chloride
1-甲基环丙烷羧酰胺盐酸盐化学式
CAS
78104-89-9
化学式
C5H10N2*ClH
mdl
MFCD09260734
分子量
134.609
InChiKey
QXMGYZRRRQGAFV-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):
    0.38
  • 重原子数:
    8
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    49.9
  • 氢给体数:
    3
  • 氢受体数:
    1

SDS

SDS:55a39640cd130d27a05fd3e34a96060a
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反应信息

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文献信息

  • Heterocyclic Compound
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20180155333A1
    公开(公告)日:2018-06-07
    The present invention provide a compound having an orexin receptor antagonistic activity, which is expected to be useful as medicaments such as agents for the prophylaxis or treatment of sleep disorder, depression, anxiety disorder, panic disorder, schizophrenia, drug dependence, Alzheimer's disease and the like. The present invention relates to a compound represented by the formula (I): wherein each symbol is as defined in the specification, or a salt thereof.
    本发明提供了一种具有促醒素受体拮抗活性的化合物,预计可用作药物,如预防或治疗睡眠障碍、抑郁症、焦虑症、恐慌症、精神分裂症、药物依赖、阿尔茨海默病等的药剂。 本发明涉及由以下式(I)表示的化合物: 其中每个符号如规范中定义,或其盐。
  • WDR5-MLL1 INHIBITORS AND MODULATORS
    申请人:Vanderbilt University
    公开号:US20200055824A1
    公开(公告)日:2020-02-20
    Benzamides and picolinamides that are meta-substituted with imino-, guanidino-, or heterocycle-containing groups disrupt the WDR5-MLL1 protein-protein interaction, and have use in pharmaceutical compositions and in treating proliferative disorders and conditions in a subject, such as cancer.
    苯甲酰胺和吡啶甲酰胺,它们在间位被亚胺基、胍基或含杂环基团取代,会破坏WDR5-MLL1蛋白质间相互作用,并可用于制药组合物中,用于治疗受试者中的增殖性疾病和状况,如癌症。
  • Organic Compounds
    申请人:Caravatti Giorgio
    公开号:US20090163469A1
    公开(公告)日:2009-06-25
    The present invention relates to compounds of formula I and its salts, wherein the substituents are as defined in the description, to compositions and use of the compounds in the treatment of diseases ameloriated by inhibition of phosphatidylinositol 3-kinase.
    本发明涉及公式I的化合物及其盐,其中取代基如描述中所定义,以及该化合物在治疗通过抑制磷脂酰肌醇3-激酶改善的疾病中的应用。
  • Phosphorus esters of alkylcycloalkyl-5-pyrimidinols and control of corn
    申请人:The Dow Chemical Company
    公开号:US04444764A1
    公开(公告)日:1984-04-24
    Compounds of the formulas: ##STR1## wherein R is alkylcycloalkyl having 4 to 6 carbon atoms; R' is hydrogen, alkyl or alkylthio of 1 to 3 carbons; R" is alkyl having 1 to 4 carbon atoms; X is oxygen or sulfur; and R'" is alkyl of 1 to 2 carbons, alkoxy, alkylthio or monoalkylamino, each with 1 to 4 carbon atoms, or phenyl. The novel 1-alkylcycloalkyl pyrimidinols are used in preparing the phosphate compounds which are highly useful corn rootworm control agents and are particularly valuable when applied to the soil, but are also useful applied to foliage of corn. Especially good control is obtained of corn rootworm. The compounds are conveniently applied in the form of a composition containing a pesticidal carrier such as an inert solvent or a finely divided inert solid in which case the composition is preferably granulated. An effective application rate is in the range of about 0.1 to about 5 pounds per acre when soil incorporated, and about 0.5 to about 2000 ppm for foliar applications.
    该化合物的分子式为:##STR1##其中R是具有4到6个碳原子的烷基环烷基;R'是氢,1到3个碳的烷基或烷基硫;R"是具有1到4个碳原子的烷基;X是氧或硫;R'"是1到2个碳的烷基,烷氧基,烷基硫或单烷基氨基,每个原子有1到4个碳,或苯环。新型的1-烷基环烷基嘧啶醇用于制备磷酸盐化合物,这些化合物是高度有效的玉米根虫控制剂,特别是在施用于土壤时非常有价值,但也适用于施用于玉米叶面。特别是对于玉米根虫的控制效果非常好。这些化合物通常以杀虫剂载体的形式施用,例如惰性溶剂或细粉惰性固体,此时,该组合物最好是颗粒状的。有效的施用速率在土壤中为每英亩约0.1到约5磅,叶面施用为约0.5到约2000 ppm。
  • Novel Hydantoin Derivatives as Metalloproteinase Inhibitors
    申请人:Gabos Balint
    公开号:US20080293743A1
    公开(公告)日:2008-11-27
    The invention provides compounds of formula (I): wherein R 1 , R 2 , A, A 1 and B are as defined in the specification; processes for their preparation; pharmaceutical compositions containing them; a process for preparing the pharmaceutical compositions; and their use in therapy. The compounds are useful as MMP inhibitors.
    本发明提供了式(I)的化合物:其中R1、R2、A、A1和B如规范中定义;它们的制备过程;含有它们的制药组合物;制备该制药组合物的过程;以及它们在治疗中的使用。这些化合物有助于作为MMP抑制剂。
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同类化合物

(N-(2-甲基丙-2-烯-1-基)乙烷-1,2-二胺) (4-(苄氧基)-2-(哌啶-1-基)吡啶咪丁-5-基)硼酸 (11-巯基十一烷基)-,,-三甲基溴化铵 鼠立死 鹿花菌素 鲸蜡醇硫酸酯DEA盐 鲸蜡硬脂基二甲基氯化铵 鲸蜡基胺氢氟酸盐 鲸蜡基二甲胺盐酸盐 高苯丙氨醇 高箱鲀毒素 高氯酸5-(二甲氨基)-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-2-甲基吡啶正离子 高氯酸2-氯-1-({(E)-[4-(二甲氨基)苯基]甲亚基}氨基)-6-甲基吡啶正离子 高氯酸2-(丙烯酰基氧基)-N,N,N-三甲基乙铵 马诺地尔 马来酸氢十八烷酯 马来酸噻吗洛尔EP杂质C 马来酸噻吗洛尔 马来酸倍他司汀 顺式环己烷-1,3-二胺盐酸盐 顺式氯化锆二乙腈 顺式吡咯烷-3,4-二醇盐酸盐 顺式双(3-甲氧基丙腈)二氯铂(II) 顺式3,4-二氟吡咯烷盐酸盐 顺式1-甲基环丙烷1,2-二腈 顺式-二氯-反式-二乙酸-氨-环己胺合铂 顺式-二抗坏血酸(外消旋-1,2-二氨基环己烷)铂(II)水合物 顺式-N,2-二甲基环己胺 顺式-4-甲氧基-环己胺盐酸盐 顺式-4-环己烯-1.2-二胺 顺式-4-氨基-2,2,2-三氟乙酸环己酯 顺式-2-甲基环己胺 顺式-2-(苯基氨基)环己醇 顺式-2-(氨基甲基)-1-苯基环丙烷羧酸盐酸盐 顺式-1,3-二氨基环戊烷 顺式-1,2-环戊烷二胺 顺式-1,2-环丁腈 顺式-1,2-双氨甲基环己烷 顺式--N,N'-二甲基-1,2-环己二胺 顺式-(R,S)-1,2-二氨基环己烷铂硫酸盐 顺式-(2-氨基-环戊基)-甲醇 顺-2-戊烯腈 顺-1,3-环己烷二胺 顺-1,3-双(氨甲基)环己烷 顺,顺-丙二腈 非那唑啉 靛酚钠盐 靛酚 霜霉威盐酸盐 霜脲氰