摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

Cyanomethoxycarbonylketene-bis-(ethyl-mercaptal) | 17823-60-8

中文名称
——
中文别名
——
英文名称
Cyanomethoxycarbonylketene-bis-(ethyl-mercaptal)
英文别名
Methyl 2-cyano-3,3-bis(ethylsulfanyl)prop-2-enoate
Cyanomethoxycarbonylketene-bis-(ethyl-mercaptal)化学式
CAS
17823-60-8
化学式
C9H13NO2S2
mdl
——
分子量
231.34
InChiKey
SZGBCJBSKKMIGK-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):
    2.3
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    101
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1-(4-(2-溴乙氧基)苯基)乙酮Cyanomethoxycarbonylketene-bis-(ethyl-mercaptal)氢氧化钾 作用下, 以46%的产率得到4-Ethylsulfanyl-6-[4-(2-ethylsulfanyl-ethoxy)-phenyl]-2-oxo-2H-pyran-3-carbonitrile
    参考文献:
    名称:
    6-Aryl-4-methylsulfanyl-2H-pyran-2-one-3-carbonitriles as PPAR-γ activators
    摘要:
    Various 6-aryl-3-cyano/methoxycarbonyl-4-methylsulfanyl-2H-pyran-2-ones have been synthesized as a potential substitute of 2,4-thiazolidinedione head group to express potent PPAR-gamma transactivation response. Some of the screened compounds have shown promising PPAR-gamma agonistic activity. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.031
点击查看最新优质反应信息

文献信息

  • [EN] SUBSTITUTED FLUORANTHENE-7-CARBONITRILES AS FLUORESCENT DYES FOR CELL IMAGING APPLICATIONS<br/>[FR] FLUORANTHÈNE-7-CARBONITRILES SUBSTITUÉS UTILISÉS EN TANT QUE COLORANTS FLUORESCENTS POUR DES APPLICATIONS D'IMAGERIE CELLULAIRE
    申请人:COUNCIL SCIENT IND RES
    公开号:WO2014147642A1
    公开(公告)日:2014-09-25
    The present invention relates to novel donor-acceptor fluoranthenes of the general formula I which can be used potentially in developing fluorescent probes, and a process of preparing said novel compounds. More particularly, the present invention relates to amine or alkoxy group as donor and nitrile group as an acceptor attached to the fluoranthene skeleton, processes for preparing the said compounds and their uses as fluorescent probes in chemical and biological sciences such as cell imaging applications, diagnostics, fluorescent tags and other useful applications. The compounds are prepared by reacting 2H-pyran-2-ones in isolated or rigid conformations with cyclic ketones containing methylene carbonyl moiety in the presence of a base in an organic solvent.
    本发明涉及一种新型供体-受体氟蒽化合物,其通式为I,可能用于开发荧光探针,并提供了制备这些新型化合物的方法。更具体地说,本发明涉及将胺或烷氧基作为供体,将腈基作为受体连接到氟蒽骨架上,制备这些化合物的方法,以及它们在化学和生物科学中作为荧光探针的用途,如细胞成像应用、诊断、荧光标记和其他有用的应用。这些化合物是通过在有机溶剂中在孤立或刚性构象下,将2H-吡喃-2-酮与含有亚甲基羰基团的环状酮在碱存在下反应而制备的。
  • 6-Aryl-4-methylsulfanyl-2H-pyran-2-one-3-carbonitriles as PPAR-γ activators
    作者:Ashoke Sharon、Ramendra Pratap、Rit Vatsyayan、Prakas R. Maulik、Uma Roy、Atul Goel、Vishnu Ji Ram
    DOI:10.1016/j.bmcl.2005.05.031
    日期:2005.7
    Various 6-aryl-3-cyano/methoxycarbonyl-4-methylsulfanyl-2H-pyran-2-ones have been synthesized as a potential substitute of 2,4-thiazolidinedione head group to express potent PPAR-gamma transactivation response. Some of the screened compounds have shown promising PPAR-gamma agonistic activity. (c) 2005 Elsevier Ltd. All rights reserved.
查看更多

同类化合物

甲酰四硫富瓦烯 环己酮,2-[二(甲硫基)亚甲基]- 5-乙基-2-甲基-噻吩-3-酮 4-羟基-2,5-二甲基噻吩-3(2H)-酮 4-乙基硫烷基-丁-3-烯-2-酮 4,4-二甲基-1,1-双(甲基硫代)-1-戊烯-3-酮 3-[双(甲基磺酰基)亚甲基]-2,4-戊二酮 3,3-双(甲硫基)-2-氰基丙烯酸乙酯 2-氰基-3,3-双(甲基硫代)丙烯酰胺 2-氰-3,3-二(甲硫基)丙烯酸甲酯 2-氯-3-氧代-2,3-二氢-2-噻吩羧酸甲酯 2-氨基-4,5-二氢-3-噻吩甲酰胺 2-乙酰基-3-氨基-3-甲基硫代丙烯腈 2-丙烯酸,3-(十六烷基硫代)-,甲基酯,(Z)- 2-(环丙基羰基)-3,3-二(甲基硫代)丙烯腈 2-(1,3-二噻戊环-2-亚基)环戊酮 2-(1,3-二噻戊环-2-亚基)环己酮 2,2-二甲基噻吩-3-酮 1-己烯-3-酮,1,1-二(甲硫基)-2-硝基- 1,3-二硫杂环戊烯-4-羧酸 (3Z)-1,1,1-三氟-4-(甲硫基)-3-丁烯-2-酮 (3E)-4-(甲硫基)-3-戊烯-2-酮 (2Z)-[3-(2-溴乙基)-4-氧代-1,3-噻唑烷-2-亚基]乙酸乙酯 (2Z)-2-(3-乙基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2Z)-(3-甲基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2E)-2-(4-氧代噻唑烷-2-亚基)乙酸丁酯 2-[bis(methylthio)methylene]-5-([13C]-methyl)cyclohexanone 2-Cyan-2-(2,3,4,5,6,7-hexahydrobenzothiazol-2-yliden)essigsaeuremethylester 2-(chlorodifluoromethylcarbonylmethylene)-1,3-thiazolidine 2,3-bis((S)-2-dodecyloxy-propanylthio)-6-(carboxy)tetrathiafulvalene 3-Amino-2-cyan-3-(ethylthio)acrylsaeuremethylester 5-dimethylaminomethylene-3-ethoxycarbonyl-2-methyl-4-oxo-4,5-dihydrothiophene 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-dithiolane 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-oxathiolane (Z)-4-(1-Butylthio)-but-3-en-2-one methyl 3-(butylthio)acrylate 3-Methylamino-3-methylmercapto-2-cyan-acrylsaeure-methylester 2-sec-butoxy-3,5-dimethylthiotetronic acid ethyl 2-amino-4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiophene-3-carboxylate cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allyl ester 2‑(3,3‑dimethyl‑2‑oxobutylidene)‑1,3‑thiazolidin‑4‑one isopropyl 1,3-dithiol-2-ylidenemethylsulfonylacetate (E)-5-(furan-2-yl)-1,1-bis(methylthio)penta-1,4-dien-3-one ethyl 3-cyclohexylamino-3-methylthio-2-cyanoacrylate ethyl 2-ethoxy-4,5-dihydrothiophene-3-carboxylate 2,4-dimethyl-2,3-dihydro-thiophen-3-one isopropyl 2-(1,3-dithiol-2-ylidene)-2-(N-cyclohexylcarbamoyl)acetate 4,4-bis(methylthio)but-3-en-2-one-1,1,1,3-d4 N-(2-aminoethyl)-benzo[b]thieno[2,3-c]pyridine-3-carboamide.hydrochloride 3-(1,3-dithiolan-2-ylidene)butan-2-one