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N-methyl 2-chlorobutanamide | 74802-82-7

中文名称
——
中文别名
——
英文名称
N-methyl 2-chlorobutanamide
英文别名
2-chloro-N-methylbutanamide
N-methyl 2-chlorobutanamide化学式
CAS
74802-82-7
化学式
C5H10ClNO
mdl
——
分子量
135.594
InChiKey
SNAOCFPIOBTDIK-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:
    250.6±23.0 °C(Predicted)
  • 密度:
    1.052±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    N-methyl 2-chlorobutanamideO,O-二甲基二硫代磷酸盐,钾盐碳酸氢钠 作用下, 生成 Di-O-methyl-S-<1-methylcarbamoyl-propyl>dithiophosphat
    参考文献:
    名称:
    O,O-Dialkyl S-(carbamoylalkyl) phosphorodithioates
    摘要:
    DOI:
    10.1021/jo01351a033
  • 作为产物:
    描述:
    参考文献:
    名称:
    N-1(2,2-二氯亚烷基)胺与氰化钾的反应:β-氯-α-氰胺,α-氯亚氨酸酯和2-氨基-5-氰的合成
    摘要:
    通过用N-氯代琥珀酰亚胺氯化脂肪族醛亚胺而制备的N-1(2,2-二氯亚烷基)胺与甲醇中过量的氰化钾反应,得到β-氯代-α-氰基烯胺。当反应进行较长时间时,分离出α-氯亚氨酸盐(Nt-Bu化合物除外)。α-氯代亚胺与氰化钾在二甲基亚砜中在70°下反应生成1,2-二氰基烯胺,而在120°下通过1,3-二氰基烯胺生成2-氨基-5-氰基吡咯。讨论了反应机理。
    DOI:
    10.1016/0040-4020(80)85035-6
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文献信息

  • Substituted heterocyclic compounds
    申请人:——
    公开号:US20040152890A1
    公开(公告)日:2004-08-05
    Disclosed are novel heterocyclic derivatives, useful for the treatment of various disease states, in particular cardiovascular diseases such as atrial and ventricular arrhythmias, intermittent claudication, Prinzmetal's (variant) angina, stable and unstable angina, exercise induced angina, congestive heart disease, and myocardial infarction. The compounds are also useful in the treatment of diabetes.
    本发明涉及新型杂环衍生物,可用于治疗各种疾病状态,特别是心血管疾病,如心房和心室心律失常、间歇性跛行、普林兹梅特尔(变异型)心绞痛、稳定和不稳定性心绞痛、运动诱发性心绞痛、充血性心力衰竭和心肌梗塞。该化合物也可用于糖尿病的治疗。
  • Substituted piperazine compounds and their use as fatty acid oxidation inhibitors
    申请人:CV THERAPEUTICS, INC.
    公开号:EP1806346A1
    公开(公告)日:2007-07-11
    Disclosed are novel heterocyclic derivatives, useful for the treatment of various disease states, in particular cardiovascular diseases such as atrial and ventricular arrhythmias, intermittent claudication, Prinzmetal's (variant) angina, stable and unstable angina, exercise induced angina, congestive heart disease, and myocardial infarction. The compounds are also useful in the treatment of diabetes.
    所公开的新型杂环衍生物可用于治疗各种疾病,尤其是心血管疾病,如房性和室性心律失常、间歇性跛行、普林兹梅塔尔(变异型)心绞痛、稳定型和不稳定型心绞痛、运动诱发心绞痛、充血性心脏病和心肌梗塞。这些化合物还可用于治疗糖尿病。
  • Polymer production method and radical polymerization initiating group-containing compound
    申请人:DAINICHISEIKA COLOR & CHEMICALS MFG. CO., LTD.
    公开号:US10982033B2
    公开(公告)日:2021-04-20
    The present invention provides: a novel production technique that enables production of a polymer whose molecular weight and molecular weight distribution are controlled and production of a polymer having a complicated structure in a desirably controlled manner using commercially available materials without using a radical polymerization initiator or a special material for use in living radical polymerization and without the need for strict polymerization conditions; and a radical polymerization initiating group-containing compound for use in the technique. The present invention relates to: a method for producing a polymer, the method including a polymerization step of mixing and warming (1) a radically polymerizable monomer, (2) an organic compound wherein at least one group that functions as a group for initiating polymerization of the monomer and that has a structure represented by formula 1 or formula 2 (X in the formula represents Cl or Br) is introduced in a molecule of the organic compound, and (3) an iodine-containing compound, thereby initiating, from the group having the structure, radical polymerization accompanied by a termination reaction; and the organic compound of (2) for use in the method.
    本发明提供了:一种新型生产技术,该技术可使用市售材料,无需使用自由基聚合引发剂或用于活自由基聚合的特殊材料,也无需严格的聚合条件,即可生产出分子量和分子量分布可控的聚合物,并以理想的可控方式生产出具有复杂结构的聚合物;以及一种用于该技术的含自由基聚合引发基团的化合物。本发明涉及一种生产聚合物的方法,该方法包括以下聚合步骤:将(1)可自由基聚合的单体;(2)有机化合物,其中在有机化合物分子中引入至少一个可作为单体聚合引发基团的基团,该基团具有式 1 或式 2 所代表的结构(式中的 X 代表 Cl 或 Br);(3)含碘化合物,从而从具有该结构的基团引发伴随终止反应的自由基聚合;以及 (2) 中的有机化合物用于该方法。
  • VERHE R.; KIMPE N. DE; BUYCK L. DE; TILLEY M.; SCHAMP N., TETRAHEDRON, 1980, 36, NO 1, 131-142
    作者:VERHE R.、 KIMPE N. DE、 BUYCK L. DE、 TILLEY M.、 SCHAMP N.
    DOI:——
    日期:——
  • SUBSTITUTED PIPERAZINE COMPOUNDS AND THEIR USE AS FATTY ACID OXIDATION INHIBITORS
    申请人:CV THERAPEUTICS, INC.
    公开号:EP1567525A2
    公开(公告)日:2005-08-31
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