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碳酸双(1-氯乙基)酯 | 50594-97-3

中文名称
碳酸双(1-氯乙基)酯
中文别名
——
英文名称
methylchloromethyl carbonate
英文别名
chloroethyl carbonate;di(chloroethyl) carbonate;Bis(1-chloroethyl) carbonate
碳酸双(1-氯乙基)酯化学式
CAS
50594-97-3
化学式
C5H8Cl2O3
mdl
——
分子量
187.023
InChiKey
MZFKWPWFMYRWPP-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:
    67-72 °C(Press: 9 Torr)
  • 密度:
    1.294±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险性防范说明:
    P305+P351+P338
  • 危险性描述:
    H227,H315,H319,H335
  • 储存条件:
    在惰性气体保护下,存储温度为2-8°C。

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] COMPOUNDS AND METHODS FOR THE TREATMENT OF OCULAR DISORDERS<br/>[FR] COMPOSÉS ET PROCÉDÉS POUR LE TRAITEMENT DE TROUBLES OCULAIRES
    申请人:AZURA OPHTHALMICS LTD
    公开号:WO2020212755A1
    公开(公告)日:2020-10-22
    Described herein are compositions and methods for the treatment of ocular surface disorders including meibomian gland dysfunction, blepharitis, dry eye disease and other inflammatory and/or infectious disease of the anterior surface of the eye. Said compositions and methods comprise keratolytic conjugates which demonstrate keratolytic activity, and anti- inflammatory or other desirable activities. Topical administration of said compositions to the eyelid margin or surrounding areas provides therapeutic benefit to patients suffering from ocular surface disorders.
    本文描述了用于治疗眼表面疾病的组合物和方法,包括睑板腺功能障碍、睑缘炎、干眼症和其他眼前表面的炎症和/或感染性疾病。所述组合物和方法包括表现出角质溶解活性的角质溶解共轭物,以及抗炎或其他理想活性。将所述组合物局部施用于眼睑边缘或周围区域可为患有眼表面疾病的患者提供治疗益处。
  • Insecticidal Benzenedicarboxamide Derivative
    申请人:Wada Katsuaki
    公开号:US20110184188A1
    公开(公告)日:2011-07-28
    The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W 1 to W 9 , and R 1 to R 3 are as defined here-in.
    本发明涉及一种新型苯二甲酰胺衍生物及其作为杀虫剂的用途,其化学式为(I),其中化学基团W1至W9,以及R1至R3如本文所定义。
  • [EN] PRODRUGS OF KALLIKREIN INHIBITORS<br/>[FR] PROMÉDICAMENTS D'INHIBITEURS DE LA KALLICRÉINE
    申请人:BIOCRYST PHARM INC
    公开号:WO2018081513A1
    公开(公告)日:2018-05-03
    Disclosed are compounds of formula I, II, and III, and pharmaceutically acceptable salts thereof, which are inhibitors of kallikrein. Also provided are pharmaceutical compositions comprising such a compound, and methods involving use of the compounds and compositions in the treatment and prevention of acquired or hereditary angioedema, or other diseases and conditions characterized by aberrant kallikrein activity. (I) (II) (III)
    公开了式I、II和III的化合物及其药学上可接受的盐,它们是激肽释放酶抑制剂。还提供了包含此类化合物的药物组合物,以及使用这些化合物和组合物治疗和预防获得性或遗传性血管性水肿或其他以异常激肽释放酶活性为特征的疾病和病症的方法。(I) (II) (III)
  • [EN] LIPID PRODRUGS OF PREGNANE NEUROSTEROIDS AND USES THEREOF<br/>[FR] PROMÉDICAMENTS LIPIDIQUES DE NEUROSTÉROÏDES DE PRÉGNANE ET LEURS UTILISATIONS
    申请人:PURETECH HEALTH LLC
    公开号:WO2020028787A1
    公开(公告)日:2020-02-06
    The present invention provides lymphatic system-directing lipid prodrugs, pharmaceutical compositions thereof, methods of producing such prodrugs and compositions, as well as methods of improving the bioavailability or other properties of a therapeutic agent that comprises part of the lipid prodrug. The present invention also provides methods of treating a disease, disorder, or condition such as those disclosed herein, comprising administering to a patient in need thereof a disclosed lipid prodrug or a pharmaceutical composition thereof.
    本发明提供了淋巴系统定向脂质前药,以及其制药组合物、生产这种前药和组合物的方法,以及改善作为脂质前药一部分的治疗剂的生物利用度或其他性质的方法。本发明还提供了治疗疾病、紊乱或症状的方法,包括向需要的患者施用所述的脂质前药或其制药组合物。
  • [EN] PHOSPHOLIPID-DETERGENT CONJUGATES AND USES THEREOF<br/>[FR] CONJUGUÉS DE PHOSPHOLIPIDE-DÉTERGENT ET LEURS UTILISATIONS
    申请人:UNIV STRASBOURG
    公开号:WO2013014073A1
    公开(公告)日:2013-01-31
    The invention relates to novel compounds, in particular novel O-substituted phospholipids that are useful for the in vitro and in vivo delivery of drugs as well as nucleic acids into cells. The invention also relates to pharmaceutical compositions and supramolecular complexes comprising said compounds and the use of these compounds in therapeutic treatment, in particular in gene therapy.
    这项发明涉及新型化合物,特别是新型O-取代磷脂类化合物,可用于体外和体内将药物以及核酸输送到细胞内。该发明还涉及包括所述化合物的药物组合物和超分子复合物,以及这些化合物在治疗治疗中的使用,特别是在基因治疗中。
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