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tert-butyl 1,3,3,3-tetrafluoro-2-methoxycarbonylpropenyl sulfide | 89563-09-7

中文名称
——
中文别名
——
英文名称
tert-butyl 1,3,3,3-tetrafluoro-2-methoxycarbonylpropenyl sulfide
英文别名
1-tert-butylthio-1,3,3,3-tetrafluoro-2-carbomethoxypropene;methyl 3-tert-butylthio-3-fluoro-2-fluoromethylacrylate;Methyl 3-t-butylthio-3-fluoro-2-trifluoromethyl-acrylate;methyl 3-tert-butylsulfanyl-3-fluoro-2-(trifluoromethyl)prop-2-enoate
tert-butyl 1,3,3,3-tetrafluoro-2-methoxycarbonylpropenyl sulfide化学式
CAS
89563-09-7
化学式
C9H12F4O2S
mdl
——
分子量
260.253
InChiKey
SELIXUWSYHRYKM-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):
    3.1
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    7

SDS

SDS:5eb8f47955b0e774ed88e446978c2181
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反应信息

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文献信息

  • ——
    作者:A. N. Kovregin、A. Yu. Sizov、A. F. Ermolov
    DOI:10.1023/a:1011325520421
    日期:——
    A new method was developed for the synthesis of fluorine-containing functionally substituted vinyl sulfides and ketene dithioacetals from the corresponding derivatives of a-trifluoromethyl-substituted CH-acids and thiols in the presence of BF(3) . NEt(3).
  • ——
    作者:A. N. Kovregin、A. Yu. Sizov、A. F. Ermolov
    DOI:10.1023/a:1019669820268
    日期:——
    alpha-Fluorine-containing beta-functionalized vinyl sulfides readily react with N-nucleophiles to form alpha-fluorine-substituted products. The reactions with phenylhydrazines and amidines of acids are accompanied by cyclization at the functional group. Thermal cyclization of cyanotrifluoromethylketene N,S-acetals proceeds at the trifluoromethyl group to give substituted 3-cyanoquinolin-4-ones.
  • ——
    作者:A. N. Kovregin、A. Yu. Sizov、A. F. Ermolov
    DOI:10.1023/a:1024781929253
    日期:——
    A new method was developed for the synthesis of methoxycarbonyltrifluoromethylthioketene by thermal cleavage of tert-butyl 1,3,3,3-tetrafluoro-2-methoxycarbonylpropenyl sulfide in the presence Of P2O5. This thioketene was demonstrated to exhibit high reactivity in reactions with nucleophiles as well as in ene and diene syntheses.
  • Dehydrohalogenation of fluorinated sulfenyl chlorides. synthesis and properties of perfluoroisobutylene sulfide
    作者:R. A. Bekker、L. A. Rozov、V. Ya. Popkova
    DOI:10.1007/bf00954716
    日期:1983.11
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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