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S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine | 229955-73-1

中文名称
——
中文别名
——
英文名称
S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine
英文别名
N-(Trifluoroacetyl)-S-methyl-S-cyclohexylsulfimine;N-[cyclohexyl(methyl)-λ4-sulfanylidene]-2,2,2-trifluoroacetamide
S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine化学式
CAS
229955-73-1
化学式
C9H14F3NOS
mdl
——
分子量
241.277
InChiKey
FUXSJMFGCDSEQQ-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):
    3.9
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    48.6
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    lithium N,O-bis(trifluoroacetyl)hydroxylamine甲基硫环己酯 在 copper(II) bis(trifluoromethanesulfonate) 作用下, 以 乙二醇二甲醚 为溶剂, 以80%的产率得到S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine
    参考文献:
    名称:
    N,O-Bis(trifluoroacetyl)hydroxylamine as a Useful Electrophilic Nitrogen Source:  Catalytic Synthesis of N-(Trifluoroacetyl)sulfilimines
    摘要:
    [GRAPHICS]In the presence of catalytic quantites of Cu(OTf)(2) the novel hydroxamic acid anhydride salt functions competently in the trifluoroacetamidation of sulfides to afford N-(trifluoroacetyl)sulfilimines. The salient features of this salt include its ease of synthesis from the inexpensive, commercially available starting materials trifluoroacetic anhydride and hydroxylamine hydrochloride.
    DOI:
    10.1021/ol9900515
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文献信息

  • PROCESS FOR PREPARING PAN-CDK INHIBITORS OF THE FORMULA (I), AND INTERMEDIATES IN THE PREPARATION
    申请人:Krüger Joachim
    公开号:US20130245261A1
    公开(公告)日:2013-09-19
    The invention relates to a novel process for the preparation of pan-CDK inhibitors of the formula (I), and intermediates of the preparation.
    这项发明涉及一种新型用于制备化合物(I)的泛CDK抑制剂的方法,以及制备过程中的中间体。
  • [DE] VERFAHREN ZUR HERSTELLUNG VON PAN-CDK-INHIBITOREN DER FORMEL (I), SOWIE INTERMEDIATE DER HERSTELLUNG<br/>[EN] PROCESS FOR PREPARING PAN-CDK INHIBITORS OF THE FORMULA (I), AND INTERMEDIATES IN THE PREPARATION<br/>[FR] PROCÉDÉ DE PRODUCTION D'INHIBITEURS PAN-CDK DE LA FORMULE (I), ET INTERMÉDIAIRE DE LA PRODUCTION
    申请人:BAYER PHARMA AG
    公开号:WO2012038411A1
    公开(公告)日:2012-03-29
    Die Erfindung betrifft ein neues Verfahren zur Herstellung von pan-CDK-Inhibitoren der Formel (I), sowie Intermediate der Herstellung.
    这项发明涉及一种制备pan-CDK抑制剂的新方法,其化学式为(I),以及其制备的中间体。
  • US9359306B2
    申请人:——
    公开号:US9359306B2
    公开(公告)日:2016-06-07
  • <i>N</i>,<i>O</i>-Bis(trifluoroacetyl)hydroxylamine as a Useful Electrophilic Nitrogen Source:  Catalytic Synthesis of <i>N</i>-(Trifluoroacetyl)sulfilimines
    作者:C. S. Tomooka、D. D. LeCloux、H. Sasaki、E. M. Carreira
    DOI:10.1021/ol9900515
    日期:1999.7.1
    [GRAPHICS]In the presence of catalytic quantites of Cu(OTf)(2) the novel hydroxamic acid anhydride salt functions competently in the trifluoroacetamidation of sulfides to afford N-(trifluoroacetyl)sulfilimines. The salient features of this salt include its ease of synthesis from the inexpensive, commercially available starting materials trifluoroacetic anhydride and hydroxylamine hydrochloride.
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同类化合物

S,S-diisopropyl-sulfimide N-tert-butyloxycarbonyl isopropyl methyl sulfimine N-trifluoroacetyl-methyl isopropylsulfilimine S,S-dipropyl-sulfimide thioaceramide S,S-bis-(2-hydroxy-ethyl)-sulfimide (Dimethyl-lambda4-sulfanylidene)urea N-Acetyliminodiethylsulfuran N-Monochloracetyl-S,S-dimethylsulfimid N-acetyl-S-methyl-S-(perfluorooctyl)sulfilimine Dimethylsulfimin prop-2-enyl N-[2-methoxyethyl(methyl)-lambda4-sulfanylidene]carbamate N-dichloroacetyl-S,S-diethylsulphilimine (4-Aminobutylsulfinimidoyl)formic acid 2-Methyl-1-sulfanylideneguanidine 2-thionitroso-1,4-dihydropyrazine 4-thionitroso-3,4-dihydro-2H-pyran 1-(1-Thionitrosopropyl)cyclohexa-1,3-diene 1-sulfanylidene-2H-pyrazin-1-ium (2-Aminoethylsulfinimidoyl)methanethial 3,6-Dimethylheptyl-imino-methyl-lambda4-sulfane Dimethyl-(2,3,5-trimethylcyclohepta-1,3,6-trien-1-yl)imino-lambda4-sulfane N'-carbamimidoyl-N-sulfanylidenemethanimidamide 2-Dodecyl-1-sulfanylideneguanidine ethane;2-thionitrosoethenamine Sulfanylidene(12-thionitrosododecylimino)-lambda4-sulfane Imino-(2-methylpropyl)-propan-2-yl-lambda4-sulfane Imino(dipentyl)-lambda4-sulfane Cyclopropyl-imino-propan-2-yl-lambda4-sulfane Imino-propan-2-yl-propyl-lambda4-sulfane Cyclobutyl-imino-propan-2-yl-lambda4-sulfane tert-butyl (NE)-N-[methyl(propan-2-yl)-lambda4-sulfanylidene]carbamate N-(dimethyl-lambda4-sulfanylidene)-2,2,2-trifluoroacetamide S-cyclohexyl-S-methyl-N-(trifluoroacetyl)sulfilimine N-acetyl dimethylsulfimide diethyl(imino)-λ4-sulfane sulfate 1-Methylsulfanyl-3-thionitrosopropane