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8-Chloroisothiochroman-4-one | 133093-52-4

中文名称
——
中文别名
——
英文名称
8-Chloroisothiochroman-4-one
英文别名
8-chloro-1H-isothiochromen-4-one
8-Chloroisothiochroman-4-one化学式
CAS
133093-52-4
化学式
C9H7ClOS
mdl
——
分子量
198.673
InChiKey
BWDUWXYNDPEABG-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):
    2.6
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2H-Thiecin, 3,4,8,9-tetradehydro-5,10-dihydro-, (Z)-四氯化碳 、 selenium(IV) oxide 、 氧气 作用下, 反应 42.0h, 以11%的产率得到2-异硫代苯并二氢吡喃-4-酮
    参考文献:
    名称:
    新型硒介导的与新carcarinostatin发色团有关的1,6-diyn-3-ene系统的芳构化
    摘要:
    1,6-二炔-3-烯系统的治疗1与SEO 2引起了迈尔斯类型环化,以产生双基6通过烯炔-丙二烯系统5,其通过的烯反应产生1与SEO 2,类似于与的新carcarinostatin发色团。
    DOI:
    10.1039/c39910000694
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文献信息

  • The manners of aromatization of a new 10-membered ring 1,6-diyn-3-ene system under basic conditions
    作者:Kazunobu Toshima、Kazumi Ohta、Tatsuya Ohtake、Kuniaki Tatsuta
    DOI:10.1016/s0040-4039(00)92636-4
    日期:1991.1
    Treatment of a novel 10-membered ring 1,6-diyn-3-ene compound 1 with alcoholic KOH solution gave isothiochromanol derivatives through a polar pathway. On the other hand, treatment of 1 with DBU in CCl4 afforded 8-chloro-isothiochromane derivatives through a free radical pathway.
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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