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1-Cyclohexyl-2-formylhydrazin | 16120-77-7

中文名称
——
中文别名
——
英文名称
1-Cyclohexyl-2-formylhydrazin
英文别名
N-(cyclohexylamino)formamide
1-Cyclohexyl-2-formylhydrazin化学式
CAS
16120-77-7
化学式
C7H14N2O
mdl
——
分子量
142.201
InChiKey
JNMXLOMKZNLYNN-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):
    1.1
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    41.1
  • 氢给体数:
    2
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • METHOD FOR PREPARING FORMAMIDE COMPOUND
    申请人:SHANGHAI GREENCARBON HI-TECH CO., LTD.
    公开号:US20180030009A1
    公开(公告)日:2018-02-01
    Disclosed is a method for preparing a formamide compound, the method uses carbon dioxide, hydrogen and an amine compound as raw materials and a transition metal complex as a catalyst, and the reaction is carried out in an organic solvent or in the absence of a solvent to form a formamide compound. The method of the present invention is an effective method of chemical utilization of carbon dioxide, which has the advantages of high reaction efficiency, a good selectivity, mild conditions, economic and environmental protection, being simple and convenient to operate and the like, and has a good popularization and application prospect.
    揭示了一种制备甲酰胺化合物的方法,该方法使用二氧化碳氢气和胺化合物作为原料,以过渡属配合物作为催化剂,并在有机溶剂中或无溶剂条件下进行反应以形成甲酰胺化合物。本发明的方法是一种有效的二氧化碳化学利用方法,具有高反应效率、良好的选择性、温和的条件、经济环保、操作简单方便等优点,具有良好的推广应用前景。
  • BICYCLIC COMPOUND, PRODUCTION AND USE THEREOF
    申请人:TOBIRA THERAPEUTICS, INC.
    公开号:US20160008326A1
    公开(公告)日:2016-01-14
    The present invention provides a new cyclic compound having a CCR antagonist activity, especially a CCR5 antagonist activity, and the use thereof. The compound of the present invention is represented by the formula: wherein, R 1 is a 5- to 6-membered ring group which may be substituted; X 1 is a bond or the like; ring A is a 5- to 6-membered ring group which may be substituted; ring B is a 8- to 10-membered ring group which may be substituted; X 2 is a bivalent group of 1 to 4 atom; Z 1 is a bivalent cyclic ring group or the like; Z 2 is a bond or the like; and R 2 is an amino group, a nitrogen-containing heterocyclic group which may be substituted or the like, or a salt thereof.
    本发明提供了一种具有CCR拮抗活性的新环化合物,特别是CCR5拮抗活性,以及其用途。本发明的化合物由以下公式表示:其中,R1是一个可能被取代的5至6成员环基团;X1是键或类似物;环A是一个可能被取代的5至6成员环基团;环B是一个可能被取代的8至10成员环基团;X2是1至4原子的二价基团;Z1是二价环状基团或类似物;Z2是键或类似物;R2是基、可能被取代的含氮杂环基团或类似物,或其盐。
  • DIOXAANTHANTHRENE-BASED COMPOUND, LAMINATED STRUCTURE AND MOLDING METHOD THEREOF, AND ELECTRONIC DEVICE AND PRODUCTION METHOD THEREOF
    申请人:Sony Corporation
    公开号:EP2767540A1
    公开(公告)日:2014-08-20
    Provided is a dioxaanthanthrene compound represented by, for example, the following structural formula (1).
    提供的是一种二氧化合物,例如,可以用以下结构式(1)表示。
  • [EN] BICYCLIC COMPOUND, PRODUCTION AND USE THEREOF<br/>[FR] COMPOSE BICYCLIQUE, PRODUCTION ET UTILISATION CORRESPONDANTES
    申请人:TAKEDA CHEMICAL INDUSTRIES LTD
    公开号:WO2003014105A1
    公开(公告)日:2003-02-20
    The present invention provides a new cyclic compound having a CCR antagonist activity, especially a CCR5 antagonist activity, and the use thereof. The compound of the present invention is represented by the formula (I) wherein: R1 is a 5- to 6-membered ring group which may be substituted; X1 is a bond or the like; ring A is a 5- to 6-membered ring group which may be substituted; ring B is a 8- to 10-membered ring group which may be substituted; X2 is a bivalent group of 1 to 4 atoms; Z1 is a bivalent cyclic ring group or the like; Z2 is a bond or the like; and R2 is an amino group, a nitrogen-containing heterocyclic group which may be substituted or the like, or a salt thereof.
    本发明提供了一种具有CCR拮抗剂活性,特别是CCR5拮抗剂活性的新的环状化合物及其用途。本发明的化合物由式(I)表示,其中:R1是可取代的5-至6-成员环基团;X1是键或类似物;环A是可取代的5-至6-成员环基团;环B是可取代的8-至10-成员环基团;X2是1至4个原子的双价基团;Z1是双价的环状环基团或类似物;Z2是键或类似物;R2是基、可能被取代的含氮杂环基团或类似物,或其盐。
  • Bicyclic compound, production and use thereof
    申请人:——
    公开号:US20040259876A1
    公开(公告)日:2004-12-23
    The present invention provides a new cyclic compound having a CCR antagonist activity, especially a CCR5 antagonist activity, and the use thereof. The compound of the present invention is represented by the formula: 1 wherein, R 1 is a 5- to 6-membered ring group which may be substituted; X 1 is a bond or the like; ring A is a 5- to 6-membered ring group which may be substituted; ring B is a 8- to 10-membered ring group which may be substituted; X 2 is a bivalent group of 1 to 4 atoms; Z 1 is a bivalent cyclic ring group or the like; Z 2 is a bond or the like; and R 2 is an amino group, a nitrogen-containing heterocyclic group which may be substituted or the like, or a salt thereof.
    本发明提供了一种具有CCR拮抗剂活性,特别是CCR5拮抗剂活性的新型环状化合物以及其用途。本发明的化合物由下式表示:1其中,R1是一个可被取代的5-至6-成员环基团;X1是一个键或类似物;环A是一个可被取代的5-至6-成员环基团;环B是一个可被取代的8-至10-成员环基团;X2是1至4个原子的双价基团;Z1是一个双价环状基团或类似物;Z2是一个键或类似物;R2是基、含氮杂环基团(可被取代)或类似物的盐。
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