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(4-甲基苯并[b]噻吩-3-基)甲醇 | 451524-34-8

中文名称
(4-甲基苯并[b]噻吩-3-基)甲醇
中文别名
——
英文名称
(4-methylbenzo[b]thiophen-3-yl)methan-1-ol
英文别名
3-hydroxymethyl-4-methyl-benzo[b]thiophene;(4-methyl-benzo[b]thiophen-3-yl)-methanol;3-hydroxymethyl-4-methylbenzo[b]thiophene;(4-Methylbenzo[b]thiophen-3-yl)methanol;(4-methyl-1-benzothiophen-3-yl)methanol
(4-甲基苯并[b]噻吩-3-基)甲醇化学式
CAS
451524-34-8
化学式
C10H10OS
mdl
——
分子量
178.255
InChiKey
KDPGPPWJUPUFPB-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:
    338.5±27.0 °C(Predicted)
  • 密度:
    1.245±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    48.5
  • 氢给体数:
    1
  • 氢受体数:
    2

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • AMINOAZOLE DERIVATIVE
    申请人:Teijin Pharma Limited
    公开号:US20190031628A1
    公开(公告)日:2019-01-31
    A compound, represented by the following formula or a medically acceptable salt thereof, having an effect of regulating the activity of an androgen receptor. In the formula, X represents S, O; Z represents (R a ) n -A- (CR 13 R 14 ) 0-1 —(CR 11 R 12 ) 0-1 ; A represents aryl, heteroaryl; R 1 represents alkyl, cycloalkyl, alkenyl, alkynyl, alkoxyalkyl, aryl, arylalkyl, heterocycle, heterocyclic alkyl; R 2 represents hydrogen, halogen, alkyl, cycloalkyl, phenyl; R3 represents hydrogen, halogen, alkyl, cycloalkyl, alkoxyalkyl, alkenyl, alkynyl, cycloalkenyl, aryl, arylalkyl, heterocycle, heterocyclic alkyl, acyl, cycloalkylcarbonyl, benzoyl, spiroalkyl, adamantyl, silyl, R 31 R 32 NCO—; R 4 and R 5 represent hydrogen, halogen, alkyl, phenyl, and cycloalkyl.
    一种化合物,由以下公式或其医学上可接受的盐表示,具有调节雄激素受体活性的作用。在公式中,X代表S,O;Z代表(R a )n-A-(CR 13 R 14 )0-1—(CR 11 R 12 )0-1;A代表芳基,杂环芳基;R1代表烷基,环烷基,烯基,炔基,烷氧基烷基,芳基,芳基烷基,杂环,杂环烷基;R2代表氢,卤素,烷基,环烷基,苯基;R3代表氢,卤素,烷基,环烷基,烷氧基烷基,烯基,炔基,环烯烯基,芳基,芳基烷基,杂环,杂环烷基,酰基,环烷基羰基,苯甲酰基,螺环烷基,金刚烷基,硅基,R31R32NCO—;R4和R5代表氢,卤素,烷基,苯基和环烷基。
  • BENZOÝb¨THIOPHEN DERIVATIVE AND PROCESS FOR PRODUCTION THEREOF
    申请人:Teijin Pharma Limited
    公开号:EP1947097A1
    公开(公告)日:2008-07-23
    The invention provides benzo[b]thiophene derivatives useful as production intermediates for chymase inhibitors, and a process for their production. The invention relates to benzo[b]thiophene derivatives represented by the following formula, and a process for their production.
    该发明提供了作为钳酶抑制剂生产中间体有用的苯并[b]噻吩衍生物,以及它们的生产方法。该发明涉及以下式表示的苯并[b]噻吩衍生物,以及它们的生产方法。
  • 3-Hydroxymethylbenzo[b]thiophene derivatives and process for their preparation
    申请人:——
    公开号:US20030191325A1
    公开(公告)日:2003-10-09
    The present invention is a method of producing a 3-hydroxymethyl-benzo[b]thiophene derivative without the possible concomitant formation of isomers, which comprises selectively cyclizing a sulfoxide having X shown in the reaction scheme below: 1 wherein R 1 to R 3 are, same or independently, a hydrogen atom, an alkyl group having 1 to 4 carbons, a trihalomethyl group, an alkoxy group having 1 to 4 carbons, an alkylthio group having 1 to 4 carbons, or a trihalomethoxy group; R 4 is an acyl group; X is a halogen atom, a hydroxy group, an amino group, a mercapto group, an alkylthio group having 1 to 9 carbons, an acyloxy group having 1 to 9 carbons, an acylamino group having 1 to 9 carbons, or a trihalomethoxy group.
    本发明是一种制备3-羟甲基苯并[b]噻吩衍生物的方法,不会伴随同构体的形成,其包括选择性地环化具有下列反应方程式中所示X的亚砜:1其中R1至R3相同或独立地是氢原子、具有1至4个碳的烷基、三卤甲基、具有1至4个碳的烷氧基、具有1至4个碳的烷硫基或三卤甲氧基;R4是酰基;X是卤原子、羟基、氨基、巯基、具有1至9个碳的烷硫基、具有1至9个碳的酰氧基、具有1至9个碳的酰胺基或三卤甲氧基。
  • Benzo(b)thiophene derivatives and process for producing the same
    申请人:——
    公开号:US20030176490A1
    公开(公告)日:2003-09-18
    The present invention is 3,4-disubstituted-benzo[b]thiophene derivatives represented by general formula (I) and processes for preparing compounds represented by general formula (V) from compounds represented by general formula (IV), preparing a mixture of compounds represented by the following formula (II) and the following formula (III) and preparing the benzo[b]thiophene derivatives represented by the above formula (I). 1 wherein, R 1 and R 2 represent each a halogen atom, a trihalomethyl group, a C 1-4 alkyl group or a C 14 alkoxy group; X represents a hydroxy group or a halogen atom; R 3 and R 4 represent each a hydrogen or a halogen atom, a trihalomethyl group, a C 1-4 alkyl group or a C 1-4 alkoxy group; and R 5 represents a C 1-3 alkyl group or a trifluoromethyl group.
    本发明涉及一种由通式(I)表示的3,4-二取代苯并[b]噻吩衍生物以及从通式(IV)表示的化合物制备通式(V)表示的化合物的过程,制备以下式(II)和以下式(III)表示的化合物的混合物,并制备上述通式(I)表示的苯并[b]噻吩衍生物。其中,R1和R2分别表示卤原子、三卤甲基基团、C1-4烷基基团或C14烷氧基团;X表示羟基或卤原子;R3和R4分别表示氢原子或卤原子、三卤甲基基团、C1-4烷基基团或C1-4烷氧基团;R5表示C1-3烷基基团或三氟甲基基团。
  • 3-Hydroxymethylbenzo[b]thiophene derivatives and process for their preparation
    申请人:Teijin Limited
    公开号:US06774245B2
    公开(公告)日:2004-08-10
    The present invention is a method of producing a 3-hydroxymethyl-benzo[b]thiophene derivative without the possible concomitant formation of isomers, which comprises selectively cyclizing a sulfoxide having X shown in the reaction scheme below: wherein R1 to R3 are, same or independently, a hydrogen atom, an alkyl group having 1 to 4 carbons, a trihalomethyl group, an alkoxy group having 1 to 4 carbons, an alkylthio group having 1 to 4 carbons, or a trihalomethoxy group; R4 is an acyl group; X is a halogen atom, a hydroxy group, an amino group, a mercapto group, an alkylthio group having 1 to 9 carbons, an acyloxy group having 1 to 9 carbons, an acylamino group having 1 to 9 carbons, or a trihalomethoxy group.
    本发明涉及一种制备3-羟甲基苯并[b]噻吩衍生物的方法,该方法不会伴随着异构体的形成,其包括选择性地环化具有下面反应方程中所示的X的亚砜:其中,R1至R3分别是氢原子、具有1到4个碳的烷基、三卤甲基、具有1到4个碳的烷氧基、具有1到4个碳的烷硫基或三卤甲氧基,且可以相同或独立;R4是酰基;X是卤原子、羟基、氨基、巯基、具有1到9个碳的烷硫基、具有1到9个碳的酰氧基、具有1到9个碳的酰胺基或三卤甲氧基。
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