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1,3-丙二醇 | 598-44-7

中文名称
1,3-丙二醇
中文别名
1,1-丙二醇;丙二醇
英文名称
(S)-(+)-propane-1,2-diol
英文别名
Propanediol;propane-1,1-diol
1,3-丙二醇化学式
CAS
598-44-7;26264-14-2
化学式
C3H8O2
mdl
——
分子量
76.0953
InChiKey
ULWHHBHJGPPBCO-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

  • LogP:
    -1.050 (est)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    5
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:a23310039130f68e17329f9408b67905
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反应信息

  • 作为反应物:
    描述:
    右旋酮洛芬1,3-丙二醇3-hydroxypropyl (2S)-2-(3-benzoylphenyl)propanoate 、 silica gel 作用下, 以to give 2.63 g (56%) of the compound 18 as a colorless oil的产率得到3-hydroxypropyl (2S)-2-(3-benzoylphenyl)propanoate
    参考文献:
    名称:
    Conjugates of dithiocarbamate disulfides with pharmacologically active agents and uses therefor
    摘要:
    根据本发明,提供了生理相容的自由基清除剂(例如,二硫代氨基甲酸盐二硫化物(DD))和药理活性剂(例如,NSAID)的共轭物。本发明的共轭物提供了一种新的药理活性剂(例如,抗炎剂),由于按照本文所述修改药理活性剂所赋予的保护作用,因此导致副作用的发生率大大降低。此外,本发明的共轭物比未经修改的药理活性剂更有效,因为当共轭物被裂解时,自由基清除剂(例如,二硫代氨基甲酸盐)与药理活性剂同时产生,从而保护了受到药理活性剂作用的细胞和组织免受自由基过度产生引起的潜在损伤。
    公开号:
    US06274627B1
  • 作为产物:
    描述:
    乳酸乙酯 在 lithium aluminium tetrahydride 作用下, 生成 (R)-1,2-丙二醇1,3-丙二醇
    参考文献:
    名称:
    Diethoxytriphenylphosphorane: a mild, regioselective cyclodehydrating reagent for conversion of diols to cyclic ethers: stereochemistry, synthetic utility, and scope
    摘要:
    DOI:
    10.1021/ja00304a030
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文献信息

  • Manufacture of gamma-butyrolactones from 1,3-glycols and esters, halides
    申请人:National Distillers and Chemical Corporation
    公开号:US04069232A1
    公开(公告)日:1978-01-17
    Gamma-butyrolactones are manufactured from olefins by reacting an olefin with an aldehyde to produce a 1,3-difunctional compound, reacting the 1,3-difunctional compound with carbon monoxide, and thereafter recovering the lactone thus produced.
    Gamma-丁内酯是通过将烯烃与醛反应产生1,3-双官能团化合物,将1,3-双官能团化合物与一氧化碳反应,然后回收生成的内酯而制造的。
  • Immunosuppressant compounds and compositions
    申请人:Marsilje H. Thomas
    公开号:US20050014724A1
    公开(公告)日:2005-01-20
    The present invention relates to immunosuppressant, process for their production, their uses and pharmaceutical compositions containing them. The invention provides a novel class of compounds useful in the treatment or prevention of diseases or disorders mediated by lymphocyte interactions, particularly diseases associated with EDG receptor mediated signal transduction.
    本发明涉及免疫抑制剂,其生产过程,其用途以及含有它们的制药组合物。该发明提供了一种新的化合物类,可用于治疗或预防由淋巴细胞相互作用介导的疾病或障碍,特别是与EDG受体介导的信号转导相关的疾病。
  • Substituted 1-(2-aryl-1,3-dioxolan-2-ylmethyl)-1H-1,2,4-triazoles
    申请人:Janssen Pharmaceutica, N.V.
    公开号:US04338327A1
    公开(公告)日:1982-07-06
    Novel 1-(2-aryl-1,3-dioxolan-2-ylmethyl)-1H-1,2,4-triazoles wherein the 1,3-dioxolane ring is substituted in the 4-position which are useful for the protection of plants and plant products against fungal attack.
    小说1-(2-芳基-1,3-二氧杂环戊烷-2-基甲基)-1H-1,2,4-三唑,其中1,3-二氧杂环戊烷环在4位被取代,对于保护植物和植物产品免受真菌攻击是有用的。
  • Piperidine Derivatives As Renin Inhibitor
    申请人:Herold Peter
    公开号:US20080076766A1
    公开(公告)日:2008-03-27
    The application relates to novel substituted piperidines of the general formula (I) in which R 1 , R 2 , R 3 , R 4 , W, X, Z, m and n are each as defined in detail in the description, to a process for their preparation and to the use of these compounds as medicines, in particular as renin inhibitors.
    该申请涉及一种新的取代哌啶,其通式为(I),其中R1、R2、R3、R4、W、X、Z、m和n在详细说明中各自定义,以及其制备方法和这些化合物作为药物的用途,特别是作为肾素抑制剂。
  • CYCLOPENTADIENYL, INDENYL OR FLUORENYL SUBSTITUTED PHOSPHINE COMPOUNDS AND THEIR USE IN CATALYTIC REACTIONS
    申请人:Plenio Herbert
    公开号:US20090253907A1
    公开(公告)日:2009-10-08
    A phosphine compound represented by general formula (1) wherein R′ and R″ independently are selected from alkyl, cycloalkyl and 2-furyl radicals, or R′ and R″ are joined together to form with the phosphorous atom a carbon-phosphorous monocycle including at least 3 carbon atoms or a carbon-phosphorous bicycle; the alkyl radicals, cycloalkyl radicals, and carbon-phosphorous monocycle being unsubstituted or substituted by at least one radical selected from the group of alkyl, cycloalkyl, aryl, alkoxy, and aryloxy radicals; Cp s is a partially substituted or completely substituted cyclopentadien-1-yl group, including substitutions resulting in a fused ring system, and wherein a substitution at the 1-position of the cyclopentadien-1-yl group is mandatory when the cyclopentadien-1-yl group is not part of a fused ring system or is part of an indenyl group. These phosphines can be used as ligands in catalytic reactions.
    一种磷化合物,其通式表示为(1),其中R'和R''独立地选择烷基,环烷基和2-呋喃基基团,或者R'和R''与磷原子结合形成至少包括3个碳原子的碳-磷单环或碳-磷双环;烷基基团,环烷基基团和碳-磷单环未经取代或被至少一种从烷基,环烷基,芳基,烷氧基和芳氧基基团组成的基团取代;Cps是部分取代或完全取代的环戊二烯-1-基基团,包括导致融合环系统的取代,当环戊二烯-1-基基团不是融合环系统的一部分或是一个茚基基团的一部分时,必须在环戊二烯-1-基基团的1位进行取代。这些磷化物可以用作催化反应中的配体。
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