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4-methyl-1-oxo-1H-isothiochromene-3-carboxylic acid | 56661-85-9

中文名称
——
中文别名
——
英文名称
4-methyl-1-oxo-1H-isothiochromene-3-carboxylic acid
英文别名
4-Methyl-1-oxo-1H-isothiochromen-3-carbonsaeure;4-methyl-1-oxo-1H-2-benzothiopyran-3-carboxylic acid;4-Methyl-2-thiaisocoumarin-3-carboxylic acid;4-methyl-1-oxoisothiochromene-3-carboxylic acid
4-methyl-1-oxo-1<i>H</i>-isothiochromene-3-carboxylic acid化学式
CAS
56661-85-9
化学式
C11H8O3S
mdl
——
分子量
220.249
InChiKey
IIVRZNNHCNKESQ-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

物化性质

  • 沸点:
    372.9±42.0 °C(Predicted)
  • 密度:
    1.432±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    79.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

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文献信息

  • 1-Oxo-1H-2-benzothiopyran-3-carboxylic acid derivatives
    申请人:Richardson-Merrell Inc.
    公开号:US03960892A1
    公开(公告)日:1976-06-01
    The method comprises administering to an animal a novel pharmaceutical composition containing a substituted-1-oxo-1H-2-benzothiopyran-3-carboxylic acid to inhibit antigen-antibody reaction in said animal. Representative of the compounds that can be used in the method are: 1-Oxo-1H-2-benzothiopyran-3-carboxylic acid, and Sodium 6-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylate.
    该方法包括向动物施用一种新型药物组合物,其中含有一种取代的-1-氧代-1H-2-苯硫杂喹-3-羧酸,以抑制该动物体内的抗原-抗体反应。可用于该方法的化合物代表包括:1-氧代-1H-2-苯硫杂喹-3-羧酸和6-甲氧基-1-氧代-1H-2-苯硫杂喹-3-羧酸钠。
  • Anti-allergic-3-carboxy-isocoumarin compositions and methods of use
    申请人:Beecham Group Limited
    公开号:US03975535A1
    公开(公告)日:1976-08-17
    3-Carboxyisocoumarins, 2-thiaisocoumarins and related isocarbostyrils are useful anti-allergic agents. Several of these compounds are novel, and a process for their preparation is provided.
    3-羧基异香豆素,2-硫异香豆素及相关的异羧基苯乙烯类化合物是有用的抗过敏剂。其中几种化合物是新颖的,并提供了它们的制备过程。
  • Pharmaceutical compositions and methods of treatment with
    申请人:Richardson-Merrell Inc.
    公开号:US04018891A1
    公开(公告)日:1977-04-19
    The method comprises administering to an animal a novel pharmaceutical composition containing a substituted-1-oxo-1H-2-benzothiopyran-3-carboxylic acid to inhibit antigen-antibody reaction in said animal. Representative of the compounds that can be used in the method are: 1-Oxo-1H-2-benzothiopyran-3-carboxylic acid, and Sodium 6-methoxy-1-oxo-1H-2-benzothiopyran-3-carboxylate.
    该方法包括向动物施用一种新的药物组合物,该组合物包含一种取代-1-氧代-1H-2-苯并硫杂吡喃-3-羧酸,以抑制该动物的抗原-抗体反应。可以用于该方法的化合物代表包括:1-氧代-1H-2-苯并硫杂吡喃-3-羧酸和6-甲氧基-1-氧代-1H-2-苯并硫杂吡喃-3-羧酸钠。
  • Isocarbostyril-3-carboxylic acid derivatives for the prophylaxis of
    申请人:Beecham Group Limited
    公开号:US04036964A1
    公开(公告)日:1977-07-19
    3-Carboxyisocoumarins, 2-thiaisocoumarins and related isocarbostyrils are useful anti-allergic agents. Several of these compounds are novel, and a process for their preparation is provided.
    3-羧基异香豆素、2-硫代异香豆素及相关的异羧基苯乙烯衍生物是有用的抗过敏药物。其中几种化合物是新颖的,并提供了它们的制备方法。
  • US3960892A
    申请人:——
    公开号:US3960892A
    公开(公告)日:1976-06-01
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同类化合物

2-溴乙酰氧基黄体酮 3-(4-propylphenyl)-1H-isothiochromene 3-(4-pentylphenyl)-1H-isothiochromene 1-(3,5-di-tert-butyl-4-hydroxyphenyl)-3-(3,4-dimethoxyphenyl)-6,7-dimethoxy-1,2-dihydro-2-thianaphthalene 2-oxide 1H-3-bromo-4-benzylthiobenzothiopyran 1-Phenyl-2-benzothiopyran-2-ium perchlorate 7-Methoxy-3-phenyl-2-benzothiopyran-2-ium perchlorate 1-(4-Chlorophenyl)-2-methyl-1H-2-benzothiopyran-2-ium perchlorate 1,2-Diphenyl-2-thiochromenium Naphtho[2,1-c]thiopyran-3-ium perchlorate Isothiochromeno[4,3-b]indol-11-ium;perchlorate (Z)-1-benzylidene-6-methoxy-3-(trifluoromethyl)-1H-isothiochromene 8,10-Dithiahexacyclo[10.6.2.13,6.02,7.09,19.016,20]henicosa-9(19),12,14,16(20),17-pentaen-11-one (Z)-1-benzylidene-7-fluoro-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-benzylidene-7-methyl-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-(4-methoxybenzylidene)-3-(trifluoromethyl)-1H-isothiochromene (Z)-1-(4-methylbenzylidene)-3-(trifluoromethyl)-1H-isothiochromene 4-(4-chlorophenyl)-6-methoxy-1H-2-benzothiopyran-1-thione 4-(4-chlorophenyl)-1H-2-benzothiopyran-1-thione 7-Methoxy-3-phenyl-2-thio-3-chromen 1-(p-Chlorphenyl)-2-thio-3-chromen 1-Phenyl-2-thio-3-chromen 1,3-Diphenyl-7-methoxy-2-thio-3-chromen 6-methoxy-4-phenyl-1H-2-benzothiopyran-1-thione 6-methoxy-4-(4-methoxyphenyl)-1H-2-benzothiopyran-1-thione 4-phenyl-1H-2-benzothiopyran-1-thione 3-(Azepane-1-carbonyl)isothiochromen-1-one 4-phenyl-1H-2-benzothiopyran 2-thianaphthylium perchlorate 4-methyl-1-oxo-1H-isothiochromene-3-carboxylic acid 3-benzoyl-2'-isopropenyl-2'-methylspiro<1H-2-benzothiopyran-1,1'-cyclopropane> 3-Phenyl-1,2-dithio-isocumarin 7,8-Dimethoxy-1-oxoisothiochromene-3-carbonyl chloride (Z)-1-benzylidene-3-(trifluoromethyl)-1H-isothiochromene 5-trifluoromethyl-1H-2-benzothiopyran-1-one Dimethyl 1-hydroxy-1-phenylisothiochromene-3,4-dicarboxylate 1-oxo-1H-isothiochromene-3-carboxylic acid (4-phenylthiazol-2-yl)amide 4-methyl-1H-benzo[h]isothiochromene 2,2-dioxide 1-formylmethylene-3-phenyl-2-benzothiopyran 4-(4-methylphenyl)-1H-2-benzothiopyran-1-thione 1,2-bis(1H-isothiochromen-3-yl)ethane benzo[c]thiopyran S,S-dioxide 3-Methoxy-1,2-dithio-isocumarin 3-iodo-4-(naphthalen-1-ylmethylsulfanyl)-1H-benzo[h]isothiochromene 1H-3-iodo-4-(4-methylbenzylthio)-6-methylbenzothiopyran 7-chloro-1-oxo-1H-isothiochromene-3-carboxylic acid 7-bromo-1-oxo-1H-isothiochromene-3-carboxylic acid 3-phenyl-1H-isothiochromen-1-one 3-(p-tolyl)-1H-isothiochromen-1-one 3-(4-chlorophenyl)-1H-isothiochromen-1-one