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N-Boc-4-isocyanatobutylamine | 851682-52-5

中文名称
——
中文别名
——
英文名称
N-Boc-4-isocyanatobutylamine
英文别名
tert-butyl N-(4-isocyanatobutyl)carbamate
N-Boc-4-isocyanatobutylamine化学式
CAS
851682-52-5
化学式
C10H18N2O3
mdl
——
分子量
214.265
InChiKey
DTSDHUMPJGCTPZ-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:
    84 °C
  • 沸点:
    320.9±25.0 °C(Predicted)
  • 密度:
    1.03±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    67.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    2-Ureidoquinoline: a useful molecular element for stabilizing single cytosine and thymine bulges
    摘要:
    We have demonstrated that aromatic heterocycles having hydrogen-bonding surfaces complementary to those of nucleotide bases are effective molecular elements for the binding to single nucleotide bulges and base mismatches. We here report that a new molecule, 2-ureidoquinoline having an alignment of hydrogen-bonding groups in the order of acceptor-donor-donor stabilizes single cytosine and thymine bulges in duplex DNAs. Furthermore, a dimeric form of 2-ureidoquinoline stabilizes cytosine-cytosine and cytosine-thymine mismatches. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.04.075
  • 作为产物:
    参考文献:
    名称:
    2-Ureidoquinoline: a useful molecular element for stabilizing single cytosine and thymine bulges
    摘要:
    We have demonstrated that aromatic heterocycles having hydrogen-bonding surfaces complementary to those of nucleotide bases are effective molecular elements for the binding to single nucleotide bulges and base mismatches. We here report that a new molecule, 2-ureidoquinoline having an alignment of hydrogen-bonding groups in the order of acceptor-donor-donor stabilizes single cytosine and thymine bulges in duplex DNAs. Furthermore, a dimeric form of 2-ureidoquinoline stabilizes cytosine-cytosine and cytosine-thymine mismatches. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.04.075
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文献信息

  • Thieno [2,3-D]pyrimidine-2,4-dione melanocortin-specific compounds
    申请人:Sharma D. Shubh
    公开号:US20050124636A1
    公开(公告)日:2005-06-09
    A thienopyrimidine compound of the formula: wherein R 1 , R 2 , R 3 , and R 4 are as defined herein, and methods of use of such compounds for the treatment of melanocortin receptor-associated disorders.
    式中的噻吩嘧啶化合物: 其中 R 1 , R 2 , R 3 和 R 4 以及使用此类化合物治疗黑色素皮质素受体相关疾病的方法。
  • NOVEL PYRROLE DERIVATIVES WITH HISTONE DEACETYLASE INHIBITOR ACTIVITY
    申请人:UNIVERSIDAD DEL PAIS VASCO-EUSKAL HERRIKO UNIBERSITATEA
    公开号:EP1975158B9
    公开(公告)日:2012-02-29
  • Synthesis and Characterization of Segmented Copoly(ether urea)s with Uniform Hard Segments
    作者:Ron M. Versteegen、Rint P. Sijbesma、E. W. Meijer
    DOI:10.1021/ma0478207
    日期:2005.4.1
    Employing protective group strategy and novel isocyanate chemistry, segmented copoly(ether urea)s with uniform hard segments were prepared. Amine-terminated poly(tetrahydrofuran) served as the soft segment of these polymers. The size of the hard segments and the number of urea groups it contains were varied systematically, and their influence on the properties was investigated. The strength of hydrogen bonding between the urea groups in monodisperse hard segments containing exactly 1 to exactly 4 urea groups was studied by infrared spectroscopy and compared with materials containing polydisperse hard segments. The strength of hydrogen bonding in polymers possessing exactly two urea groups per hard segment resulted in an optimal balance between excellent mechanical properties and good processability and solubility.
  • Pyrrolic Derivatives with Histone Deacetylase Inhibitory Activity
    申请人:Cossio Mora Fernando Pedro
    公开号:US20080262073A1
    公开(公告)日:2008-10-23
    The invention describes new compounds derived from formula I pyrroles, methods for obtaining them and their application as drugs in pharmaceutical compositions for the treatment of cancer due to their inhibitory activity on certain histone deacetylases.
  • US7638550B2
    申请人:——
    公开号:US7638550B2
    公开(公告)日:2009-12-29
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