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1,3-dimethylpyrimidinone | 94220-08-3

中文名称
——
中文别名
——
英文名称
1,3-dimethylpyrimidinone
英文别名
1,3-dimethyl-3,4-dihydro-1H-pyrimidin-2-one;1,3-dimethyltetrahydropyrimidin-2-one;1,3-dimethyltetrahydropyrimidin-2-(1H)-one;1,3-dimethyl-4H-pyrimidin-2-one
1,3-dimethylpyrimidinone化学式
CAS
94220-08-3
化学式
C6H10N2O
mdl
——
分子量
126.158
InChiKey
SFLZYXZRWZUTSC-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):
    -0.3
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    23.6
  • 氢给体数:
    0
  • 氢受体数:
    1

文献信息

  • Method and compositions for identifying anti-HIV therapeutic compounds
    申请人:Arimilli N. Murty
    公开号:US20050239054A1
    公开(公告)日:2005-10-27
    Methods are provided for identifying anti-HIV therapeutic compounds substituted with carboxyl ester or phosphonate ester groups. Libraries of such compounds are screened optionally using the novel enzyme GS-7340 Ester Hydrolase. Compositions and methods relating to GS-7340 Ester Hydrolase also are provided.
    提供了一种识别含有羧酸酯或磷酸酯基团取代的抗HIV治疗化合物的方法。可以选择使用新型酶GS-7340酯解酶对这类化合物库进行筛选。还提供了与GS-7340酯解酶相关的组合物和方法。
  • [EN] INTERMEDIATES AND METHODS FOR MAKING ZEARALENONE MACROLIDE ANALOGS<br/>[FR] INTERMÉDIAIRES ET PROCÉDÉS DE FABRICATION D'ANALOGUES MACROLIDES DE ZÉARALÉNONE
    申请人:EISAI R&D MAN CO LTD
    公开号:WO2009075818A1
    公开(公告)日:2009-06-18
    Disclosed herein are methods and intermediates useful in the preparation of macrolides, e.g., compounds of formula (IV) wherein R1-R12 are as defined herein.
    本文披露了在制备大环内酯类化合物中有用的方法和中间体,例如,公式(IV)中R1-R12所定义的化合物。
  • Oxazolidinone derivatives with antibiotic activity
    申请人:——
    公开号:US20030216373A1
    公开(公告)日:2003-11-20
    Compounds of the formula (I), or a pharmaceutically acceptable salt, or an in-vivo-hydrolysable ester thereof, 1 wherein HET is an N-linked 5-membered heteroaryl ring, optionally substituted on a C atom by an oxo or thioxo group; and/or by 1 or 2 (1-4C)alkyl groups; and/or on an available nitrogen atom by (1-4C)alkyl; or HET is an N-linked 6-membered heteroaryl ring containing up to three nitrogen heteroatoms in total, optionally substituted on a C atom as above; Q is selected from, for example, Q1 2 R 2 and R 3 are independently hydrogen or fluoro; T is selected from a range of groups, for example, of formula (TC 5 ) 3 wherein Rc is, for example, R 13 CO—, R 13 SO 2 — or R 13 CS—; wherein R 13 is, for example, optionally substituted (1-10C)alkyl or R 14 C(O)O(1-6C)alkyl wherein R 14 is optionally substituted (1-10C)alkyl; are useful as antibacterial agents; and processes for their manufacture and pharmaceutical compositions containing them are described.
    公式(I)的化合物,或其药学上可接受的盐,或其体内解酯,其中HET是一个N-连接的5-成员杂环芳基环,可选地在碳原子上被氧化或代氧基取代;和/或由1或2个(1-4C)烷基基团取代;和/或在一个可用的氮原子上由(1-4C)烷基基团取代;或者HET是一个N-连接的6-成员杂环芳基环,总共包含最多三个氮杂原子,可选地在碳原子上如上所述取代;Q是选自,例如,Q12R2和R3独立地是氢或;T是选自一系列基团,例如,如下式(TC5)3其中Rc是,例如,R13CO—,R13SO2—或R13CS—;其中R13是,例如,可选地取代的(1-10C)烷基或R14C(O)O(1-6C)烷基,其中R14是可选地取代的(1-10C)烷基;作为抗菌剂是有用的;并描述了它们的制备方法和含有它们的药物组合物。
  • [EN] ADDUCT BETWEEN A PYRROLIC COMPOUND AND AN INORGANIC OXIDE HYDROXIDE, A SUPER-ADDUCT BETWEEN A PYRROLIC COMPOUND, AN INORGANIC OXIDE HYDROXIDE AND A CARBON ALLOTROPE, ELASTOMERIC COMPOSITION COMPRISING THE SUPER-ADDUCT AND METHODS FOR PRODUCING THE SAME<br/>[FR] PRODUIT D'ADDITION ENTRE UN COMPOSÉ PYRROLIQUE ET UN HYDROXYDE D'OXYDE INORGANIQUE, UN SUPER-PRODUIT D'ADDITION ENTRE UN COMPOSÉ PYRROLIQUE, UN HYDROXYDE D'OXYDE INORGANIQUE ET UN ALLOTROPE DE CARBONE, COMPOSITION ÉLASTOMÈRE COMPRENANT LE SUPER-PRODUIT D'ADDITION ET LEURS PROCÉDÉS DE PRODUCTION
    申请人:PIRELLI
    公开号:WO2019162873A1
    公开(公告)日:2019-08-29
    Adduct obtainable by interacting: a. a pyrrolic compound of general formula (I) wherein the significance of the substituents is specified in the description and in the claims, and b. an inorganic oxide hydroxide, comprising an oxide and/or a hydroxide, wherein the ratio between the weight of said inorganic oxide hydroxide and said pyrrolic compound is greater than or equal to 10.
    通过相互作用可获得的加合物:a. 通式(I)中的吡咯化合物,其中取代基的意义在描述和权利要求中指定,并且b. 一种无机氧化物羟化物,包括氧化物和/或羟化物,其中所述无机氧化物羟化物的重量与所述吡咯化合物的重量之比大于或等于10。
  • [EN] ADDUCTS OF PYRROLE DERIVATIVES TO CARBON ALLOTROPES<br/>[FR] PRODUITS D'ADDITION DE DÉRIVÉS DE PYRROLE À DES ALLOTROPES DE CARBONE
    申请人:PIRELLI
    公开号:WO2018087685A1
    公开(公告)日:2018-05-17
    Adducts are described formed between pyrrole derivatives of formula (I) an carbon allotropes in which the carbon is sp2 hybridized, such as for example carbon nanotubes, graphene or nanographites, carbon black. The pyrrole derivatives bear substituents on the nitrogen atom suitable for improving the physicochemical characteristics of said allotropes. A process for preparing said adducts is also described. The adducts are formed with a pyrrole of formula (I) wherein X is selected from the group consisting of : The other substituents are as defined in the claims.
    加合物是在公式(I)的吡咯生物和碳异质体之间形成的,其中碳是sp2杂化的,例如碳纳米管、石墨烯或纳米石墨,碳黑。吡咯生物在氮原子上带有适合改善所述异质体的物理化学特性的取代基。还描述了制备所述加合物的方法。与公式(I)中X从以下群组中选择的吡咯形成加合物:其他取代基如权利要求中所定义。
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