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(Z)-3-(chloromethylene)-6-fluoroisothiochroman-4-one | 1251530-94-5

中文名称
——
中文别名
——
英文名称
(Z)-3-(chloromethylene)-6-fluoroisothiochroman-4-one
英文别名
(3Z)-3-(chloromethylidene)-6-fluoro-1H-isothiochromen-4-one
(Z)-3-(chloromethylene)-6-fluoroisothiochroman-4-one化学式
CAS
1251530-94-5
化学式
C10H6ClFOS
mdl
——
分子量
228.674
InChiKey
HBHVEYAHSVMHMM-WTKPLQERSA-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
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • PREPARATION AND APPLICATION OF NOVEL ANTIBACTERIAL AND ANTICANCER COMPOUNDS AND THEIR DERIVATIVES
    申请人:Yang Gengliang
    公开号:US20120035206A1
    公开(公告)日:2012-02-09
    Novel antibiotic and anticancer compounds of formula I, II, III, IV, derivatives, ostereoisomer, racemic and noracemic mixture of ostereoisomer, or the pharmaceutically acceptable salts or solvates of these compounds are disclosed. The preparation, pharmaceutical composition and biological activity of these compounds are disclosed.
    本发明揭示了化学式I、II、III、IV、衍生物、对映异构体、外消旋和非外消旋对映异构体混合物,或这些化合物的药学上可接受的盐或溶剂化物的新型抗生素和抗癌化合物。本发明还揭示了这些化合物的制备、制药组合物和生物活性。
  • PREPARATION AND APPLICATION OF THE NEW ANTIBACTERIAL AND ANTICANCER COMPOUNDS AND THEIR DERIVATIVES
    申请人:YANG Gengliang
    公开号:US20140296285A1
    公开(公告)日:2014-10-02
    A method of inhibiting microorganism growth comprising administering an effective amount of a composition including a compound selected from the group consisting of to the microorganism.
    一种抑制微生物生长的方法,包括向微生物施加包含以下化合物中的一种所选的组合物的有效量。
  • PREPARATION AND USE OF NOVEL ANTIBIOTIC, ANTICANCER COMPOUNDS AND DERIVATIVES THEREOF
    申请人:Yang, Gengliang
    公开号:EP2423213A1
    公开(公告)日:2012-02-29
    Novel antibiotic and anticancer compounds compounds of formula I, II, III, IV, derivatives , stereoisomer , racemic and noracemic mixture of stereoisomer , or the pharmaceutically acceptable salts or solvates of these compounds are disclosed. The preparation, pharmaceutical composition and biological activity of these compounds are disclosed.
    本研究公开了新型抗生素和抗癌化合物式 I、II、III、IV、衍生物、立体异构体、立体异构体的外消旋和去消旋混合物或这些化合物的药学上可接受的盐或溶液。公开了这些化合物的制备方法、药物组成和生物活性。
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同类化合物

6-溴-3,4-二氢-2H-异硫代色烯-4-胺盐酸盐 6-溴-3,4-二氢-1H-S,S-二氧代异硫色烯-4-氨基盐酸盐 4-氨基异硫代苯并二氢吡喃2,2-二氧化物盐酸盐 3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-S,S-二-氧代-异硫基苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-2-苯并噻喃 2-异硫代苯并二氢吡喃-4-酮 1H-2-苯并噻喃-4-醇,3,4-二氢- (9ci)-3,4-二氢-1H-2-苯并硫代吡喃-1-羰酰氯 (4r)-(9ci)-6-乙基-3,4-二氢-1H-2-苯并硫代吡喃-4-胺,2,2-二氧化物 isothiochroman-1-yl-methyl-amine Isothiochroman-carbonsaeure-(1)-methylester 1-methyl-1H-2-benzothiopyran-1-carbonitrile 1-Methylenisothiochroman-2,2-dioxid 3,4-dihydro-1-vinyl-1H-2-benzothiopyran N-(2,4-Dinitro-phenyl)-N'-[(S)-1-methyl-isothiochroman-(4Z)-ylidene]-hydrazine 1,1'-Bis-(4,5-dihydro-1-oxy-2H-3-benzothiepin-3,3-dioxid)thiokohlensaeure-O,O-diester pyrrolidine-1-carboxylic acid isothiochroman-1-ylamide 1-(Chlormethyl)-isothiochroman-2,2-dioxid 4,5-Dihydro-2H-3-benzothiepin-1-on-2-thiocarbonsaeure-S-methylester isothiochroman-1-yl-carbamic acid ethyl ester piperidine-1-carbothioic acid isothiochroman-1-ylamide piperidine-1-carboxylic acid isothiochroman-1-ylamide 4,5-dihydro-benzo[d]thiepin-1-one semicarbazone 1-ethyl-3-isothiochroman-1-yl-thiourea 1-isothiochroman-1-yl-3-methyl-thiourea 2-(Methylen-dithiomethylen)-4,5-dihydro-2H-3-benzothiepin-1-on-3,3-dioxid 2-Benzyliden-4,5-dihydro-2H-3-benzothiepin-1-on methyl spiro[benzo[c]thiophene-1(3H),4'-piperidine]-1'-carboxylate 2,2-dioxide 1-hydroxy-3-isothiochroman-1-yl-urea 2-(N-p-Chlorphenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 1-isothiochroman-1-yl-3-methyl-urea di-isothiochroman-1-yl-amine 2-(N-Cyclohexyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on isothiochroman-1-yl-carbamic acid methyl ester 3-isothiochroman-1-yl-1,1-dimethyl-urea N-Isothiochroman-1-yl-N-methyl-formamide 2-(N-Phenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 4-isothiochroman-1-yl-semicarbazide 4,5-Dihydro-2H-3-benzothiepin-1-on-2-dithiocarbonsaeuremethylester 2-[2-Isothiochroman-(4Z)-ylidene-ethyl]-2-methyl-cyclopentane-1,3-dione 4-Hydroxy-4-vinylthiochroman 2-Methyl-2-{2-[6-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 1-Methyl-1-carbamoyl-isothiochroman-2,2-dioxid 1-Deutero-1-cyano-isothiochroman morpholine-4-carbothioic acid isothiochroman-1-ylamide Dimethylaminomethyl-1-cyan-isothiochroman 1-Diethylaminomethyl-1-cyan-isothiochroman 2-Methyl-2-{2-[7-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 55-((trimethylsilyl)ethynyl)-3,7-dithia-1(1,3),5(1,4)-dibenzenacyclooctaphane-12,15-dicarbonitrile