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1,1-二异丙基脲 | 77464-05-2

中文名称
1,1-二异丙基脲
中文别名
——
英文名称
N,N-diisopropylurea
英文别名
Diisopropylurea;1,1-diisopropylurea;N,N-Diisopropyl-harnstoff;N,N-bis(1-methylethyl)-urea;N,N-Bis(1-methylethyl)urea;1,1-di(propan-2-yl)urea
1,1-二异丙基脲化学式
CAS
77464-05-2
化学式
C7H16N2O
mdl
MFCD01676333
分子量
144.217
InChiKey
ORHBGEQYIZTYHV-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

  • 沸点:
    202.9±23.0 °C(Predicted)
  • 密度:
    0.943±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.857
  • 拓扑面积:
    46.3
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:ab2e40f524fe4cc3d596eb6574a91885
查看

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Malik, Abdul; Afza, Nighat; Siddiqui, Salimuzzaman, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1982, vol. 37, # 4, p. 512 - 518
    摘要:
    DOI:
  • 作为产物:
    描述:
    二异丙胺盐酸 作用下, 以 乙醚氯仿 为溶剂, 反应 1.0h, 生成 1,1-二异丙基脲
    参考文献:
    名称:
    Malik, Abdul; Afza, Nighat; Siddiqui, Salimuzzaman, Zeitschrift fur Naturforschung, Teil B: Anorganische Chemie, Organische Chemie, 1982, vol. 37, # 4, p. 512 - 518
    摘要:
    DOI:
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文献信息

  • [EN] BACKBONE-CYCLIZED PEPTIDOMIMETICS<br/>[FR] PEPTIDOMIMÉTIQUES À SQUELETTE CYCLISÉ
    申请人:POLYPHOR AG
    公开号:WO2016162127A1
    公开(公告)日:2016-10-13
    Novel backbone-cyclized peptidomimetics of the general formula cyclo[-P1-P2-P3-P4-P5-P6-P7-P8-T1-T2-] (I) wherein the single elements T or P are α-amino acid residues connected in either direction which, depending on their positions in the chain, are as defined in the description and the claims, and salts thereof, have the property to modulate the GLP-1 receptor. They can be used as medicaments to treat, prevent, or delay the onset of diseases, disorders or conditions in which modulation of the human GLP-1 receptor is beneficial, such as type 2 diabetes. These backbone-cyclized peptidomimetics can be manufactured by a process which is based on a mixed solid- and solution phase synthetic strategy.
    新型的骨架环化肽类似物的一般公式为cyclo[-P1-P2-P3-P4-P5-P6-P7-P8-T1-T2-](I),其中单个元素T或P是α-氨基酸残基,以任一方向连接,根据它们在链中的位置,在描述和权利要求中定义,以及其盐,具有调节GLP-1受体的特性。它们可用作药物治疗、预防或延缓调节人类GLP-1受体有益的疾病、紊乱或病况,如2型糖尿病。这些骨架环化肽类似物可通过基于混合固相和溶液相合成策略的过程制造。
  • LANTHANIDE CLUSTERS AND METHODS OF USE THEREOF
    申请人:YEDA RESEARCH AND DEVELOPMENT CO. LTD.
    公开号:US20160002269A1
    公开(公告)日:2016-01-07
    The present invention is directed to multinuclear lanthanides chiral clusters, based on phenyl-oxazoline-amide (POxA) ligands, and to methods of use thereof. The chiral clusters of this invention are highly fluorescent with high stability.
    本发明涉及基于苯基-噁唑啉酰胺(POxA)配体的多核镧系手性簇以及其使用方法。本发明的手性簇具有高荧光性能和高稳定性。
  • Anti-Viral Compounds
    申请人:DeGoey David A.
    公开号:US20100317568A1
    公开(公告)日:2010-12-16
    Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.
    描述了一种有效抑制丙型肝炎病毒(“HCV”)复制的化合物。本发明还涉及制备这种化合物的方法、包含这种化合物的组合物,以及使用这种化合物治疗HCV感染的方法。
  • DIARYLMETHYLAMIDE DERIVATIVE HAVING ANTAGONISTIC ACTIVITY ON MELANIN-CONCENTRATING HORMONE RECEPTOR
    申请人:Banyu Pharmaceutical Co., Ltd.
    公开号:EP2272841A1
    公开(公告)日:2011-01-12
    [Problem] To provide a melanin-concentrating hormone receptor antagonist useful as a pharmaceutical agent for central diseases, circulatory diseases, and metabolic diseases. [Means for Resolution] Provided is a diarylmethylamide derivative represented by formula (I): Wherein R1a, R1b, R2a, R2b, R3a, and R3b independently represent a hydrogen atom or the like, R4 represents a hydrogen atom, C1-6 alkyl, or the like, R5 represents a hydrogen atom or the like, Z represents C1-6 alkyl or the like, or R4 and Z together form a 4- to 6-membered nitrogen-containing hetero ring, Y1 represents H or the like, Y2 represents H, or Y1 and Y2 together form - O-CH2-, W represents C, SO, or the like, Ar1 represents 6-membered aryl or the like, Ar2 represents 6-membered aryl or the like, and ring A represents a benzene ring, a pyridine ring, or the like.
    [问题] 提供一种对黑色素浓缩激素受体拮抗剂,用作中枢疾病、循环疾病和代谢疾病的药用制剂。 [解决方法] 提供一种由式(I)表示的二芳基甲酰胺衍生物: 其中R1a、R1b、R2a、R2b、R3a和R3b独立地表示氢原子或类似物,R4表示氢原子、C1-6烷基或类似物,R5表示氢原子或类似物,Z表示C1-6烷基或类似物,或者R4和Z一起形成一个含氮杂环的4-至6-成员环,Y1表示H或类似物,Y2表示H,或者Y1和Y2一起形成-O-CH2-,W表示C、SO或类似物,Ar1表示6-成员芳基或类似物,Ar2表示6-成员芳基或类似物,环A表示苯环、吡啶环或类似物。
  • [EN] MODULATORS OF HCV REPLICATION<br/>[FR] MODULATEURS DE LA REPLICATION DE HCV
    申请人:ANGELETTI P IST RICHERCHE BIO
    公开号:WO2006038039A1
    公开(公告)日:2006-04-13
    The present invention is directed to the use of compounds of formula (I): 1 R X 3 R Y ( I) 2 R 5 where X, Y, R1, R2 and R3 are defined therein, which can act as modulators of viral replication and/or virus production, especially of the hepatitis C virus (HCV), in a cell based system.
    本发明涉及使用式(I)的化合物:1 R X 3 R Y ( I) 2 R 5,其中X、Y、R1、R2和R3在其中被定义,这些化合物可以作为病毒复制和/或病毒产生的调节剂,特别是对丙型肝炎病毒(HCV)在基于细胞的系统中。
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