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3,5-二氯苯磺酸 | 33469-47-5

中文名称
3,5-二氯苯磺酸
中文别名
——
英文名称
3,5-dichloro-benzenesulfonic acid
英文别名
3,5-dichlorobenzenesulfonate;3,5-dichlorobenzenesulfonic Acid
3,5-二氯苯磺酸化学式
CAS
33469-47-5
化学式
C6H4Cl2O3S
mdl
——
分子量
227.068
InChiKey
IJJUDUDQGIIQOO-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

  • 密度:
    1.668

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    62.8
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3,5-dichloro-N-methyl-N-nitrobenzenesulfonamide 生成 3,5-二氯苯磺酸
    参考文献:
    名称:
    DROZDOVA, O. A.;ASTRATEV, A. A.;KUZNETSOV, L. L.;SELIVANOV, V. F., ZH. ORGAN. XIMII, 1983, 19, N 4, 761-766
    摘要:
    DOI:
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文献信息

  • [EN] UREA SUBSTITUTED SULPHONAMIDE DERIVATIVES<br/>[FR] DERIVES DE SULFONAMIDE SUBSTITUES PAR UREE
    申请人:BIOTIE THERAPIES CORP
    公开号:WO2010146236A1
    公开(公告)日:2010-12-23
    The present invention relates to sulphonamide derivatives, whith a urea moiety. The invention also relates to the use of the derivatives as inhibitors of collagen receptor integrins, especially α2β1 integrin inhibitors e.g. in connection with diseases and medical conditions that involve the action of cells and platelets expressing collagen receptors, their use as a medicament, e.g. for the treatment of thrombosis, inflammation, cancer and vascular diseases, pharmaceutical compositions containing them and a process for preparing them. The sulphonamide derivatives have the general formula (I) or (I').
    本发明涉及含有脲基的磺胺类衍生物。该发明还涉及将这些衍生物用作胶原受体整合素的抑制剂,特别是α2β1整合素抑制剂,例如在涉及表达胶原受体的细胞和血小板的疾病和医疗状况中使用,其用作药物,例如用于治疗血栓形成、炎症、癌症和血管疾病,含有它们的药物组合物以及制备它们的方法。这些磺胺类衍生物具有一般式(I)或(I')。
  • THIOPYRANOSE COMPOUND AND METHOD FOR PRODUCING SAME
    申请人:FUJIFILM Corporation
    公开号:US20160355497A1
    公开(公告)日:2016-12-08
    There is provided a production method of a thiopyranose compound represented by the following Formula (2) by reacting a compound represented by the following Formula (1) with a sulfur compound. X represents a leaving group. A represents an oxygen atom or a sulfur atom. Further, each of R 1A to R 4B , R 1B to R 4B , and R 5 represents a hydrogen atom or a specific substituent.
    提供了一种通过将以下式(1)代表的化合物与硫化合物反应来制备由以下式(2)表示的硫代吡喃糖化合物的生产方法。X代表一个离去基团。A代表一个氧原子或硫原子。此外,R1A到R4B,R1B到R4B和R5分别代表氢原子或特定取代基。
  • PREPARATION METHOD OF OPTICALLY ACTIVE DIAMINE COMPOUND
    申请人:Daiichi Sankyo Company, Limited
    公开号:US20160016974A1
    公开(公告)日:2016-01-21
    The problem to be solved is to provide a method for efficiently producing compounds (1) and (1a) that are important intermediate compounds in the production of FXa inhibitors (X) and (X-a). The solutions thereto are a method for producing a compound represented by the formula (8d) using a stereoselective intramolecular cyclization reaction, and a method for producing a compound (1f) or a salt thereof, or a hydrate thereof, which is characterized by desulfonylation of the compound (8d). In each formula, R 4a represents a C1-C6 alkyl group, a benzyl group, etc.
    需要解决的问题是提供一种高效生产FXa抑制剂(X)和(X-a)的重要中间化合物(1)和(1a)的方法。其解决方案是使用立体选择性分子内环化反应生产由公式(8d)表示的化合物的方法,并通过去磺酰化化合物(8d)生产化合物(1f)或其盐或水合物的方法。在每个公式中,R4代表C1-C6烷基,苄基等。
  • Nitrogen-containing heterocyclic compound
    申请人:Murakata Chikara
    公开号:US20090054407A1
    公开(公告)日:2009-02-26
    The present invention provides a nitrogen-containing heterocyclic compound represented by formula (I): wherein W represents a nitrogen atom or —CH—; X represents —C(═O)— or —CHR 4 — (wherein R 4 represents a hydrogen atom, or the like); R 1 represents a group represented by the following formula: [wherein Q 1 represents a nitrogen atom or —CR 8 — (wherein R 8 represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like). Q 2 represents —NR 15 — (wherein R 15 represents a hydrogen atom, or the like) and R 5 and R 6 may be the same or different and each represents a hydrogen atom, substituted or unsubstituted lower alkyl, or the like]; and R 2 and R 3 may be the same or different and each represents a hydrogen atom, halogen, substituted or unsubstituted lower alkyl, or the like} or a pharmaceutically acceptable salt thereof, and the like.
    本发明提供了一种含氮杂环化合物,其由式(I)表示:其中W代表氮原子或—CH—;X代表—C(═O)—或—CHR4—(其中R4代表氢原子或类似物);R1代表由以下式表示的基团:[其中Q1代表氮原子或—CR8—(其中R8代表氢原子、取代或未取代的低级烷基或类似物)。Q2代表—NR15—(其中R15代表氢原子或类似物),R5和R6可以相同也可以不同,每个代表氢原子、取代或未取代的低级烷基或类似物];R2和R3可以相同也可以不同,每个代表氢原子、卤素、取代或未取代的低级烷基或类似物}或其药学上可接受的盐等。
  • BIPYRIDINE COMPOUND, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCTION OF CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX
    申请人:Asaumi Taku
    公开号:US20100184978A1
    公开(公告)日:2010-07-22
    A bipyridine compound represented by the formula (1): wherein R 1 , R 2 and R 3 each independently represent a C1-C10 alkyl group which may be substituted etc., and R 4 , R 5 , R 6 , R 7 and R 8 each independently represent a hydrogen atom etc., a transition metal complex obtained by contacting a bipyridine compound represented by the formula (1) with a compound of a transition metal belonging to Group 9, 10 or 11, and a method for production of a conjugated aromatic compound comprising reacting an aromatic compound (A) wherein one or two leaving groups are bonded to an aromatic ring with an aromatic compound (A) having the same structure as that of the above-mentioned aromatic compound (A) or an aromatic compound (B) being structurally different from the above-mentioned aromatic compound (A) and having one or two leaving groups bonded to an aromatic ring, in the presence of the transition metal complex.
    一种以式(1)表示的联吡啶化合物:其中R1、R2和R3各自独立地表示可以被取代的C1-C10烷基等,而R4、R5、R6、R7和R8各自独立地表示氢原子等,通过将式(1)表示的联吡啶化合物与属于9、10或11族过渡金属的化合物接触而获得的过渡金属配合物,以及一种制备共轭芳香化合物的方法,包括在过渡金属配合物的存在下,将一个或两个离去基团与芳环结合的芳香化合物(A)与具有与上述芳香化合物(A)相同结构的芳香化合物(A)或结构不同于上述芳香化合物(A)且具有一个或两个离去基团与芳环结合的芳香化合物(B)反应。
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