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5-hydroxy-2,4,6,7-tetramethyl-1,3-benzoxathiole | 100480-15-7

中文名称
——
中文别名
——
英文名称
5-hydroxy-2,4,6,7-tetramethyl-1,3-benzoxathiole
英文别名
2,4,6,7-Tetramethyl-benzo[1,3]oxathiol-5-ol;2,4,6,7-tetramethyl-1,3-benzoxathiol-5-ol
5-hydroxy-2,4,6,7-tetramethyl-1,3-benzoxathiole化学式
CAS
100480-15-7
化学式
C11H14O2S
mdl
——
分子量
210.297
InChiKey
JEVCAUPKMUPVEK-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

  • 熔点:
    125-127 °C
  • 沸点:
    337.8±42.0 °C(Predicted)
  • 密度:
    1.192±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.4
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    54.8
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    5-hydroxy-2,4,6,7-tetramethyl-1,3-benzoxathiole苯甲酰氯吡啶 为溶剂, 反应 24.0h, 以to give 1.8 g of the title compound, melting at 100°-102° C.的产率得到5-Benzoyloxy-2,4,6,7-tetramethyl-1,3-benzoxathiole
    参考文献:
    名称:
    Lipid peroxide lowering 1,3-benzoxathiole derivative compositions and
    摘要:
    化合物式(I):##STR1## 其中:R.sup.1代表氢原子、烷基、取代烷基、C.sub.2-C.sub.6烯基、芳基、取代芳基或烷氧羰基基团,其中烷氧部分具有1至6个碳原子;R.sup.2代表氢原子、C.sub.1-C.sub.6烷基或C.sub.3或C.sub.4烯基;R.sup.3代表氢原子或C.sub.1-C.sub.6烷基;R.sup.4代表羟基、C.sub.1-C.sub.21脂肪酰氧基团或环状芳基羧基芳氧基团;R.sup.5代表C.sub.1-C.sub.12烷基、C.sub.1-C.sub.6烷氧基、羟基、C.sub.1-C.sub.7脂肪酰氧基团或环状芳基羧基脂肪酰氧基团;R.sup.6代表氢原子、C.sub.1-C.sub.6烷基或C.sub.1-C.sub.6烷氧基;n为0、1或2;以及其药学上可接受的盐在治疗循环障碍和过敏方面具有价值。
    公开号:
    US04871762A1
  • 作为产物:
    描述:
    三甲基氢醌吡啶二氯化二硫sodium methylate铁粉溶剂黄146 作用下, 以 甲醇乙腈 为溶剂, 反应 41.0h, 生成 5-hydroxy-2,4,6,7-tetramethyl-1,3-benzoxathiole
    参考文献:
    名称:
    Studies on hindered phenols and analogs. 2. 1,3-Benzoxathioles having SRS-A inhibiting activity
    摘要:
    A series of hindered phenolic 1,3-benzoxathioles (7a-l) were prepared and investigated for biological properties. Many compounds had LPO-lowering, antisuperoxide inhibiting, SRS-A inhibiting, and 5-lipoxygenase inhibiting activities. Among them, 5-hydroxy-4,6,7-trimethyl-2-propyl-1,3-benzoxathiole (7d) and 3-(5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiol-2-yl)propanol (7j) were most potent in SRS-A inhibiting and 5-lipoxygenase inhibiting activities, respectively, and were selected for further development as candidate drugs for the treatment of asthma.
    DOI:
    10.1021/jm00167a032
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文献信息

  • 1,3-benzoxathiole derivatives
    申请人:Sankyo Company, Limited
    公开号:US04691027A1
    公开(公告)日:1987-09-01
    Compounds formula (I): ##STR1## in which: R.sup.1 represents a hydrogen atom, an alkyl group, a substituted alkyl group, a C.sub.2 -C.sub.6 alkenyl group, an aryl group, a substituted aryl group or an alkoxycarbonyl group wherein the alkoxy part has from 1 to 6 carbon atoms; R.sup.2 represents a hydrogen atom, a C.sub.1 -C.sub.6 alkyl group or a C.sub.3 or C.sub.4 alkenyl group; R.sup.3 represents a hydrogen atom or a C.sub.1 -C.sub.6 alkyl group; R.sup.4 represents a hydroxy group, a C.sub.1 -C.sub.21 aliphatic acyloxy group or a carbocyclic aryl carboxylic acyloxy group; R.sup.5 represents a C.sub.1 -C.sub.12 alkyl group, a C.sub.1 -C.sub.6 alkoxy group, a hydroxy group, a C.sub.1 -C.sub.7 aliphatic acyloxy group or a carbocyclic aryl carboxylic acyloxy group; R.sup.6 represents a hydrogen atom, a C.sub.1 -C.sub.6 alkyl group or a C.sub.1 -C.sub.6 alkoxy group; and n is 0, 1, or 2; and pharmaceutically acceptable salts thereof are valuable in the treatment of circulatory disorders and allergies.
    化合物公式(I):##STR1##其中:R.sup.1代表氢原子,烷基,取代烷基,C.sub.2-C.sub.6烯基,芳基,取代芳基或者烷氧羰基,其中烷氧部分含有1至6个碳原子;R.sup.2代表氢原子,C.sub.1-C.sub.6烷基或者C.sub.3或C.sub.4烯基;R.sup.3代表氢原子或者C.sub.1-C.sub.6烷基;R.sup.4代表羟基,C.sub.1-C.sub.21脂肪族酰氧基或者环烷基芳基羧酰氧基;R.sup.5代表C.sub.1-C.sub.12烷基,C.sub.1-C.sub.6烷氧基,羟基,C.sub.1-C.sub.7脂肪族酰氧基或者环烷基芳基羧酰氧基;R.sup.6代表氢原子,C.sub.1-C.sub.6烷基或者C.sub.1-C.sub.6烷氧基;n为0、1或2;以及其药学上可接受的盐在治疗循环障碍和过敏症方面具有价值。
  • 1, 3-Benzoxathiole derivatives, their use and their preparation
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0157603A2
    公开(公告)日:1985-10-09
    Compounds of formula (I): in which: R1 represents a hydrogen atom, an alkyl group, a substituted alkyl group, a C2-C6 alkenyl group, an aryl group, a substituted aryl group or a (C1-C6 alkoxycarbonyl group; R2 represents a hydrogen atom, a C1-C6 alkyl group or a C3 or C4 alkenyl group; R3 represents a hydrogen atom or a C1-C6 alkyl group; R4 represents a hydroxy group, a C1-C21 aliphatic acyloxy group or an aromatic acyloxy group; R5 represents a C1-C12 alkyl group, a C1-C6 alkoxy group, a hydroxy group, a C1-C7 aliphatic acyloxy group or an aromatic acyloxy group; R6 represents a hydrogen atom, a C1-C6 alkyl group or a C1-C6 alkoxy group; and n is 0, 1, or 2; and pharmaceutically acceptable salts thereof are valuable in the treatment of circulatory disorders and allergies.
    式(I)化合物: 其中 R1 代表氢原子、烷基、取代的烷基、C2-C6 烯基、芳基、取代的芳基或 C1-C6 烷氧基羰基; R2 代表氢原子、C1-C6 烷基或 C3 或 C4 烯基; R3 代表氢原子或 C1-C6 烷基;R4 代表羟基、C1-C21 脂肪族酰氧基或芳香族酰氧基; R5 代表 C1-C12 烷基、C1-C6 烷氧基、羟基、C1-C7 脂肪族酰氧基或芳香族酰氧基; R6 代表氢原子、C1-C6 烷基或 C1-C6 烷氧基;以及 n 是 0、1 或 2; 及其药学上可接受的盐类在治疗循环系统疾病和过敏症方面具有重要价值。
  • YOSHIOKA, TAKAO;KITAZAWA, EIICHI;YAMAZAKI, MITSUO;IIZUKA, YOSHIO
    作者:YOSHIOKA, TAKAO、KITAZAWA, EIICHI、YAMAZAKI, MITSUO、IIZUKA, YOSHIO
    DOI:——
    日期:——
  • US4691027A
    申请人:——
    公开号:US4691027A
    公开(公告)日:1987-09-01
  • US4871762A
    申请人:——
    公开号:US4871762A
    公开(公告)日:1989-10-03
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同类化合物

四碘-2-磺基苯酸酐 四溴-2-磺基苯甲酸环酐 N,N'-二[[(1,3-苯并氧硫杂环戊烷-2-基)硫代]甲基]脲 5-羟基-4,6,7-三甲基-2-丙基-1,3-苯并氧杂噻唑 3-(5-羟基-4,6,7-三甲基-1,3-苯并氧杂噻唑-2-基)丙醇 2-磺基苯甲酸酐 2-(2-甲氧基丙烷-2-基)-7,7-二甲基-4-叔-丁基-8-氧杂-9-硫杂双环[4.3.0]壬-2,4,10-三烯 1,3-苯并噁噻唑,5-甲氧基-,3,3-二氧化 5,7-dimethyl-2-(2,2,2-trifluoro-1-methoxycarbonylethylidene)-1,3-benzooxathiole trans-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide trans-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide (2R,SS)-2-[(1S)-1-(4-methylphenyl)-1-(4-methoxyphenylamino)-methyl]-1,3-benzoxathiole 3(2H)-oxide 3,3-bis<(4-dimethylamino)phenyl>-4H-2,1-benzoxathiole 1-oxide 6-methyl-3,3-bis(4-dimethylaminophenyl)-3H-2,1-benzoxathiole 1-oxide (S)-6-(4-((R)-1-(5-ethylpyrimidin-2-yl)pyrrolidin-3-yl)methoxy-3-fluorophenyl)-2H-benzo[d][1,3]oxathiole 3-oxide 1,3-benzoxathiol-6-ol 1,3-benzoxathiol-6-ol-3-oxide 3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate 5-(5-t-butyldimethylsilyloxy-4,6,7-trimethyl-1,3-benzoxathiole-2-yl)-2,2-dimethylpentanoic acid trans-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide spiro<1,3-benzoxathiole-2,1'-cyclohexane> 3-oxide 4-Amino-3,3-dioxo-3λ6-benz[1,3]oxathiol-5-ol 6-Fluoro-1,3-benzoxathiol-2-amine 3H-2,1-Benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(2-ethoxyethoxy)ethoxy)ethoxy)- 4-[2-(4-Chloro-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-chloro-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-1,3-benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(4-chlorophenoxy)ethoxy)ethoxy)- 4-[2-(4-Methoxy-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-methoxy-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-2H-benzo[d][1,3]oxathiole 3,3-dioxide 4-(2-Methyl-benzo[1,3]dithiol-2-yl)-2-(2-methyl-benzo[1,3]oxathiol-2-yl)-1H-pyrrole 2,5-bis<2-(2-tert-butyl-1,3-benzoxathiolyl)>pyrrole 5-bromo-2-phenylbenzo[d][1,3]oxathiole 5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole 5-Ethoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 5-Butoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 2-t-Butyl-1,3-benzoxathiole 2-methyl-5'-nitrospiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 2,5'-dimethylspiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'-spirobi<3H-2,1-benzoxathiole> 1-oxide 3-imino-3H-2,1-benzoxathiole-1,1-dioxide Bis-(2-carboxyphenyl)-Schwefel-dihydroxid-dilacton 6-tert-Butyl-1,1,2a,4,4-pentamethyl-2a,4-dihydro-1H-2,3-dioxa-2aλ4-thia-cyclopenta[cd]indene 2,2-dimethyl-6-oxo-8-phenyl-2H,6H-<1,2>thioxolo<4,5,1-hi>benzthioxole 2-(5-Tert-butyl-3,3-dimethyl-2,1-benzoxathiol-7-yl)propan-2-ol 9-tert-Butyl-2,2,4,6,6-pentamethyl-3,5-dioxa-4λ4-thia-tricyclo[5.3.1.04,11]undeca-1(10),7(11),8-triene 4-oxide 2-(5-tert-Butyl-1-chloro-1,3,3-trimethyl-1,3-dihydro-1λ4-benzo[c][1,2]oxathiol-7-yl)-propan-2-ol