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4-(2-氯-1-甲基乙基)吗啉盐酸盐 | 76191-26-9

中文名称
4-(2-氯-1-甲基乙基)吗啉盐酸盐
中文别名
——
英文名称
4-(2-chloro-1-methyl-ethyl)-morpholine
英文别名
4-(β-chloro-isopropyl)-morpholine;4-(β-Chlor-isopropyl)-morpholin;4-(1-Chloropropan-2-yl)morpholine
4-(2-氯-1-甲基乙基)吗啉盐酸盐化学式
CAS
76191-26-9
化学式
C7H14ClNO
mdl
MFCD12030778
分子量
163.647
InChiKey
PTZCJFNGSYXQBD-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:
    88-91 °C(Press: 10 Torr)
  • 密度:
    1.0910 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    10
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12.5
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2934999090

SDS

SDS:44d516d95b5b466ef4ebaad80224c134
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反应信息

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文献信息

  • Indole nitriles
    申请人:——
    公开号:US20040077646A1
    公开(公告)日:2004-04-22
    Compounds of the formula (I) 1 wherein m, n, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as described herein, together with methods for making the compounds and using the compounds for treatment of diseases or conditions mediated by Cathepsin K.
    式(I)的化合物,其中m、n、R1、R2、R3、R4、R5和R6如本文所述,以及制备这些化合物的方法和利用这些化合物治疗由Cathepsin K介导的疾病或症状的方法。
  • Electrochemical fluorination of aminoalkyl ethers
    作者:G.G.I. Moore、J.C. Hansen、T.M. Barrett、J.E. Waddell、K.M. Jewell、T.A. Kestner、R.M. Payfer
    DOI:10.1016/s0022-1139(00)80506-0
    日期:1986.6
    trialkylamines in liquid HF takes place readily in good yields, whereas dialkyl ethers give low yields. The latter fluorinated ethers are of interest for their low temperature properties. Our goal in this work was to prepare fluorinated aminoalkyl ether fluids which might combine the favorable yields of amines and properties of ethers. Several dialkylamine and alkylene units were combined in a variety of diamino
    已知在液体HF中三烷基胺的电化学化容易以良好的产率发生,而二烷基醚的产率很低。后者的化醚因其低温性能而受到关注。我们在这项工作中的目标是制备化的基烷基醚流体,该流体可以结合胺的良好收率和醚的性能。将几种二烷基胺和亚烷基单元结合在各种二基单醚,二二醚和单基单醚中。在第一类材料中,电化学化产率高达50%。描述了这些新流体的结构-屈服关系和性质。
  • 6-membered heteroaromatic substituted cyanoindoline derivatives as NIK inhibitors
    申请人:Janssen Pharmaceutica NV
    公开号:US11001569B2
    公开(公告)日:2021-05-11
    The present invention relates to pharmaceutical agents of formula (I), useful for therapy and/or prophylaxis in a mammal, and in particular to inhibitors of NF-κB-inducing kinase (NIK—also known as MAP3K14) useful for treating diseases such as cancer, inflammatory disorders, metabolic disorders and autoimmune disorders. The invention is also directed to pharmaceutical compositions comprising such compounds, and to the use of such compounds or pharmaceutical compositions for the prevention or treatment of diseases such as a cancer, inflammatory disorders, metabolic disorders including obesity and diabetes, and autoimmune disorders.
    本发明涉及式(I)的药物制剂,可用于哺乳动物的治疗和/或预防,尤其涉及NF-κB诱导激酶(NIK-又称MAP3K14)的抑制剂,可用于治疗癌症、炎症性疾病、代谢性疾病和自身免疫性疾病等疾病。本发明还涉及包含此类化合物的药物组合物,以及使用此类化合物或药物组合物预防或治疗癌症、炎症性疾病、代谢紊乱(包括肥胖和糖尿病)和自身免疫性疾病等疾病。
  • Pesson,M. et al., Chimica Therapeutica, 1966, vol. 1, p. 127 - 136
    作者:Pesson,M. et al.
    DOI:——
    日期:——
  • AXMEDOV, SH. T.;AXUNDOVA, M. A.;SADYXOV, N. S., IZV. VUZOV. XIMIYA I XIM. TEXNOL., 1982, 25, N 7, 903-906
    作者:AXMEDOV, SH. T.、AXUNDOVA, M. A.、SADYXOV, N. S.
    DOI:——
    日期:——
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