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邻苯二甲酸氢钠 | 827-27-0

中文名称
邻苯二甲酸氢钠
中文别名
邻苯二甲酸钠盐;苯二甲酸氢钠
英文名称
Phthalic Acid Disodium Salt
英文别名
——
邻苯二甲酸氢钠化学式
CAS
827-27-0;15968-01-1;10197-71-4
化学式
C8H6NaO4
mdl
——
分子量
189.12
InChiKey
DFLCZDIXTAAMLZ-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2916399090
  • 危险性防范说明:
    P261,P271,P304+P340,P312,P403+P233,P405,P501
  • 危险性描述:
    H335

SDS

SDS:882a5873d369de84ba4cc9ea60c002b1
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制备方法与用途

用途:在中和法中作为基准,配制缓冲溶液,以及用于有机合成。

文献信息

  • Water soluble prodrugs of COX-2 inhibitors
    申请人:Payne E. Joseph
    公开号:US20060189682A1
    公开(公告)日:2006-08-24
    Disclosed are water soluble compounds which are useful as prodrugs of COX-2 inhibitors, and pharmaceutical compositions comprising them.
    揭示了作为COX-2抑制剂的前药有用的溶性化合物,以及包含它们的药物组合物。
  • [EN] PRODRUGS OF MYELOPEROXIDASE INHIBITORS<br/>[FR] PROMÉDICAMENTS D'INHIBITEURS DE LA MYÉLOPEROXYDASE
    申请人:BIOHAVEN THERAPEUTICS LTD
    公开号:WO2021072140A1
    公开(公告)日:2021-04-15
    Disclosed are prodrugs of myeloperoxidase (MPO) inhibitors, methods of treating MPO related disorders, e.g., multiple system atrophy, amyotrophic lateral sclerosis, and Huntingtons disease, and methods of neuroprotection, which include administering to a patient in need thereof the prodrugs, pharmaceutical compositions including the prodrugs, and kits including the pharmaceutical compositions and instructions for use.
    揭示了髓过氧化物酶(MPO)抑制剂的前药,治疗MPO相关疾病的方法,例如多系统萎缩症、肌萎缩侧索硬化和亨廷顿病,以及神经保护方法,包括向需要的患者施用前药,包括前药的药物组合物,以及包括药物组合物和使用说明的工具包。
  • [EN] POLYETHYLENE GLYCOL CONJUGATES OF HETEROCYCLOALKYL CARBOXAMIDO PROPANOIC ACIDS<br/>[FR] CONJUGUES A BASE DE POLYETHYLENE GLYCOL D'ACIDES HETEROCYCLOALKYL CARBOXAMIDO PROPANOIQUES
    申请人:ELAN PHARM INC
    公开号:WO2005070921A1
    公开(公告)日:2005-08-04
    Disclosed are conjugates which bind VLA-4. Certain of these conjugates also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such conjugates are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheimer’s disease, atherosclerosis, AIDS, dementia, diabetes, inflammatory bowel disease, rheumatoid arthritis, tissue transplantation, tumor metastasis and myocardial ischemia. The conjugates can also be administered for the treatment of inflammatory brain diseases such as multiple sclerosis.
    公开的是结合VLA-4的偶联物。其中一些偶联物还抑制白细胞粘附,尤其是VLA-4介导的白细胞粘附。这类偶联物可用于治疗哺乳动物患者,如人类的炎症性疾病,例如哮喘、阿尔茨海默病、动脉粥样硬化、艾滋病、痴呆、糖尿病、炎症性肠病、类风湿性关节炎、组织移植、肿瘤转移和心肌缺血。这些偶联物还可用于治疗炎症性脑病,如多发性硬化症。
  • Multimeric VLA-4 antagonists comprising polymer moieties
    申请人:Konradi W. Andrei
    公开号:US20060013799A1
    公开(公告)日:2006-01-19
    Disclosed are conjugates which bind VLA-4. Certain of these conjugates also inhibit leukocyte adhesion and, in particular, leukocyte adhesion mediated by VLA-4. Such conjugates are useful in the treatment of inflammatory diseases in a mammalian patient, e.g., human, such as asthma, Alzheimer's disease, atherosclerosis, AIDS dementia, diabetes, inflammatory bowel disease, rheumatoid arthritis, tissue transplantation, tumor metastasis and myocardial ischemia. The conjugates can also be administered for the treatment of inflammatory brain diseases such as multiple sclerosis.
    公开的是结合VLA-4的偶联物。其中一些偶联物还能抑制白细胞粘附,特别是VLA-4介导的白细胞粘附。这类偶联物可用于治疗哺乳动物患者,如人类的炎症性疾病,例如哮喘、阿尔茨海默病、动脉粥样硬化、艾滋病痴呆、糖尿病、炎症性肠病、类风湿性关节炎、组织移植、肿瘤转移和心肌缺血。这些偶联物还可用于治疗炎症性脑病,如多发性硬化症。
  • Method of separating imide compound
    申请人:——
    公开号:US20020169331A1
    公开(公告)日:2002-11-14
    A reaction product and an imide compound can be separated from a reaction mixture obtained by reacting a substrate in the presence of the imide compound having an imide unit represented by the following formula (1): 1 wherein X represents an oxygen atom, a hydroxyl group or an acyloxy group by (A1) a solvent-crystallization step for crystallizing the imide compound with at least one solvent selected from the group consisting of a hydrocarbon, a chain ether and water, (A2) a cooling-crystallization step for crystallizing the reaction product by cooling, or (B) an extraction step for distributing the reaction product into a phase of a water-insoluble solvent and the imide compound into a phase of an aqueous solvent, respectively by using the aqueous solvent containing at least water and the water-insoluble solvent separable from the aqueous solvent. Further, the imide compound and the metal catalyst can be separated from a mixture containing the imide compound and the metal catalyst by (C) a solvent-crystallization step for crystallizing the imide compound by using a solvent for crystallization, (D) an absorption step for absorbing the metal catalyst by an absorption treatment, or (E) an extraction step for distributing the imide compound into a phase of a water-insoluble solvent and the metal catalyst into a phase of an aqueous solvent, respectively by using the aqueous solvent containing at least water and the water-insoluble solvent separable from the aqueous solvent.
    一种反应产物和一种亚酰亚胺化合物可以从通过在亚酰亚胺化合物存在的情况下将底物反应得到的反应混合物中分离出来,该亚酰亚胺化合物具有以下式(1)所表示的亚酰亚胺单元: 1 其中X代表氧原子、羟基或酰氧基 通过(A1)用羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和等羟烃、链醚和
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫