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1,1,1,4-四氯-丁-3-烯-2-酮 | 83959-34-6

中文名称
1,1,1,4-四氯-丁-3-烯-2-酮
中文别名
——
英文名称
1,1,1,4-tetrachloro-but-3-en-2-one
英文别名
1,1,1,4-Tetrachlor-but-3-en-2-on;(Z)-1,1,1,4-tetrachlorobut-3-en-2-one
1,1,1,4-四氯-丁-3-烯-2-酮化学式
CAS
83959-34-6
化学式
C4H2Cl4O
mdl
——
分子量
207.871
InChiKey
HNGQOPGMEIHEGS-UPHRSURJSA-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):
    2.7
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • Method for the Production of N-Substituted (3-Dihalomethyl-1-Methyl-Pyrazole-4-yl) Carboxamides
    申请人:Zierke Thomas
    公开号:US20100174094A1
    公开(公告)日:2010-07-08
    The present invention relates to a process for preparing N-substituted (3-dihalomethylpyrazol-4-yl)carboxamides of the formula (I) in which R 1 is optionally substituted phenyl or C 3 -C 7 -cycloalkyl, R 1a is hydrogen or fluorine, or R 1a together with R 1 is optionally substituted C 3 -C 5 -alkanediyl or C 5 -C 7 -cycloalkanediyl, R 2 is C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl or C 1 -C 4 -alkoxy-C 1 -C 2 -alkyl, X is F or Cl and n is 0, 1, 2 or 3; which comprises A) providing a compound of the formula (II) in which X is F or Cl, Y is Cl or Br and R 2 has one of the meanings given above and B) reacting a compound of the formula (II) with carbon monoxide and a compound of the formula (III) in which R 1 , R 1a and n have one of the meanings given above; in the presence of a palladium catalyst; to intermediates used for the preparation according to the process according to the invention, and also to processes for their preparation.
    本发明涉及一种制备式(I)的N-取代(3-二卤甲基吡唑-4-基)羧酰胺的方法 其中R1是可选的取代苯基或C3-C7环烷基,R1a是氢或氟,或者R1a与R1一起是可选的取代C3-C5-烷二基或C5-C7-环烷二基,R2是C1-C6-烷基,C2-C6-烯基,C2-C6-炔基或C1-C4-烷氧基-C1-C2-烷基,X是F或Cl,n为0、1、2或3;包括 A)提供式(II)的化合物 其中X是F或Cl,Y是Cl或Br,R2具有上述给定的含义之一 B)将式(II)的化合物与一氧化碳和式(III)的化合物反应 其中R1、R1a和n具有上述给定的含义之一;在钯催化剂的存在下; 用于根据本发明的方法制备的中间体,以及用于它们的制备的方法。
  • Phosphate and Calcium Uptake by Rat Odontoblast-Like MRPC-1 Cells Concomitant With Mineralization
    作者:P. Lundquist、H. H. Ritchie、K. Moore、T. Lundgren、A. Linde
    DOI:10.1359/jbmr.2002.17.10.1801
    日期:——
    It has been suggested that odontoblasts are instrumental in translocating Ca2+ and inorganic phosphate (Pi) ions during the mineralization of dentin. The aim of this study was to characterize cellular Pi and Ca2+ uptake in the novel rat odontoblast‐like cell line mineralizing rat pulpal cell line (MRPC) 1 during mineralization to see if changes in the ion transport activity would occur as the cultures develop and begin forming a mineralized matrix. MRPC‐1 cells were cultured in chemically defined medium containing ascorbate and Pi, and cultures were specifically analyzed for cellular Pi and Ca2+ uptake activities and expression of type II high‐capacity Na+‐Pi cotransporters. The odontoblast‐like phenotype of the cell line was ascertained by monitoring the expression of collagen type I and dentin phosphopoprotein (DPP). Mineralized nodule formation started at day 9 after confluency and then rapidly increased. Ca2+ uptake by the cells showed a maximum during the end of the proliferative phase (days 5–7). Pi uptake declined to a basal level during proliferation and then was up‐regulated simultaneously with the onset of mineralization to a level fourfold of the basal uptake, suggesting an initiating and regulatory role for cellular Pi uptake in mineral formation. This up‐regulation coincided with a conspicuously increased glycosylation of NaPi‐2a, indicating an activation of this Na+‐Pi cotransporter. The study showed that MRPC‐1 cells express an odontoblast‐like phenotype already at the onset of culture, but that to mineralize the collagenous extracellular matrix (ECM) that formed, a further differentiation involving their ion transporters is necessary.
    有研究表明,牙本质细胞在牙本质矿化过程中有助于Ca2+和无机磷酸盐(Pi)离子的转运。本研究的目的是描述新型大鼠牙本质细胞样细胞系矿化大鼠牙髓细胞系(MRPC)1在矿化过程中的细胞Pi和Ca2+摄取特征,以了解离子转运活性是否会随着培养物的发展和矿化基质的形成而发生变化。MRPC-1细胞在含有抗坏血酸和Pi的化学定义培养基中培养,并专门分析细胞Pi和Ca2+摄取活性以及II型高容量Na+-Pi共转运蛋白的表达。通过监测I型胶原蛋白和牙本质磷蛋白(DPP)的表达来确定细胞系的牙本质细胞样表型。矿化结节形成于融合后第9天开始,然后迅速增加。细胞对Ca2+的摄取在增殖期结束时(第5-7天)达到最大值。Pi摄取在增殖期间下降到基础水平,然后在矿化开始时同步上调,达到基础摄取水平的四倍,这表明细胞Pi摄取在矿化形成中起启动和调节作用。这种上调与NaPi-2a糖基化显着增加相吻合,表明这种Na+-Pi共转运蛋白被激活。研究表明,MRPC-1细胞在培养开始时就已经表现出牙本质细胞样表型,但为了使形成的胶原细胞外基质(ECM)
  • Roedig; Becker, Justus Liebigs Annalen der Chemie, 1955, vol. 597, p. 214,224
    作者:Roedig、Becker
    DOI:——
    日期:——
  • VERFAHREN ZUR HERSTELLUNG N-SUBSTITUIERTER (3-DIHALOMETHYL-1-METHYL-PYRAZOL-4-YL)CARBOXAMIDE
    申请人:BASF SE
    公开号:EP2164831B1
    公开(公告)日:2013-07-17
  • US8153820B2
    申请人:——
    公开号:US8153820B2
    公开(公告)日:2012-04-10
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