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4-Acetamino-4.5.6.7-tetrahydro-benzothiophen | 58094-12-5

中文名称
——
中文别名
——
英文名称
4-Acetamino-4.5.6.7-tetrahydro-benzothiophen
英文别名
N-acetyl-4,5,6,7-tetrahydrobenzo[b]thiophen-4-amine;N-Acetyl-4,5,6,7-tetrahydrobenzo[b]thien-4-amine;N-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)-acetamide;N-(4,5,6,7-tetrahydro-benzo[b]thiophen-4-yl)-acetamide;N-(4,5,6,7-Tetrahydro-benzo[b]thiophen-4-yl)-acetamid;N-(4,5,6,7-tetrahydro-1-benzothiophen-4-yl)acetamide
4-Acetamino-4.5.6.7-tetrahydro-benzo<b>thiophen化学式
CAS
58094-12-5
化学式
C10H13NOS
mdl
——
分子量
195.285
InChiKey
VAXZXGLXBDGUOY-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:
    402.5±24.0 °C(Predicted)
  • 密度:
    1.18±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    57.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:4bc68725294dafdf7d0271f0e57953c1
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上下游信息

  • 下游产品
    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:
    参考文献:
    名称:
    Process for preparing 4,5,6,7-tetrahydro-7-oxobenzo[b]thiophenes and
    摘要:
    提供了一种制备某些4,5,6,7-四氢-7-氧基苯并[b]噻吩或某些1,2,3,4-四氢-4-氧基萘的酰胺或脲衍生物的过程,该过程可用作动物生长调节剂。该过程包括:在钴催化剂存在下氧化具有以下式的化合物:其中R.sub.1和R.sub.2分别是从羰基C.sub.1-C.sub.7、卤代烷基C.sub.1-C.sub.7、羧烷氧基C.sub.1-C.sub.4、和R.sub.3选自氢和烷基C.sub.1-C.sub.4的取代基组成的羧基;R.sub.4选自氢、烷基C.sub.1-C.sub.8、羰基C.sub.2-C.sub.4、卤代烷基(C.sub.2-C.sub.4)、和当##STR5##基团环化时,每个代表从琥珀酰亚胺、马来酰亚胺和邻苯二甲酰亚胺组成的基团;X和Y分别是从氢、氟、氯、溴、碘、硝基、烷基C.sub.1-C.sub.4组成的基团中选择的基团;它们的外消旋混合物和光学异构体。
    公开号:
    US04332724A1
  • 作为产物:
    描述:
    乙酸酐 、 alkaline earth salt of/the/ methylsulfuric acid 生成 4-Acetamino-4.5.6.7-tetrahydro-benzothiophen
    参考文献:
    名称:
    Synthesis of 4-Substituted Thianaphthene Derivatives
    摘要:
    DOI:
    10.1021/jo50017a009
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文献信息

  • Compositions containing 4,5,6,7-tetrahydrobenz[b]thien-4-yl-ureas or
    申请人:American Cyanamid Company
    公开号:US04036979A1
    公开(公告)日:1977-07-19
    This disclosure describes a novel method for improving feed efficiency and accelerating the growth rate of veterinary homothermic animals by administering to said animals a growth-promoting amount of a cycloalkano[b]thien-4-ylurea or thiourea.
    这份披露描述了一种新颖的方法,通过向兽医同温动物投予一定量的环戊烷基硫代脲或硫脲,以提高饲料效率并加快生长速度。
  • 1-Benzoyl-3-(4,5,6,7-tetrahydrobenzo [b]thien-4-yl)ureas and
    申请人:American Cyanamid Company
    公开号:US04053484A1
    公开(公告)日:1977-10-11
    This invention relates to 1-benzoyl-3-(4,5,6,7-tetrahydrobenzo[b]thien-4-yl)urea, 1-benzoyl-3-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)urea, and derivatives thereof and a method for the preparation of said compounds and substituted derivatives. Both of the above referred-to compounds are novel and useful intermediates for the preparation of the corresponding tetrahydrobenzo[b]thien-4-ylurea and tetrahydro-7-oxobenzo[b]thien-4-ylurea, respectively. The latter compounds and certain derivatives thereof are animal growth promoting agents.
    本发明涉及1-苯甲酰基-3-(4,5,6,7-四氢苯并[b]噻吩-4-基)脲、1-苯甲酰基-3-(4,5,6,7-四氢-7-氧代苯并[b]噻吩-4-基)脲及其衍生物以及制备该化合物及其取代衍生物的方法。上述两种化合物均为新颖且有用的中间体,可用于制备相应的四氢苯并[b]噻吩-4-基脲和四氢-7-氧代苯并[b]噻吩-4-基脲。后者及其某些衍生物是动物生长促进剂。
  • Process for preparation 4,5,6,7-tetrahydro-7-oxobenzo-[b]-thiophenes and
    申请人:American Cyanamid Company
    公开号:US04254268A1
    公开(公告)日:1981-03-03
    There is provided an oxidation process using potassium permanganate as oxidizing agent, for the preparation of certain animal growth promoters, namely, N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)amides, 4,5,6,7-tetrahydro-7-oxobenzo[b]-thien-4-ylureas, N-(1,2,3,4-tetrahydro-4-oxo-1-naphthyl)amides and 1,2,3,4-tetrahydro-4-oxo-1-naphthylureas, said process affording such compounds in markedly improved yields, and being readily suitable for scale-up.
    提供了一种使用高锰酸钾作为氧化剂的氧化过程,用于制备某些动物生长促进剂,即N-(4,5,6,7-四氢-7-氧代苯并[b]噻吩-4-基)酰胺,4,5,6,7-四氢-7-氧代苯并[b]噻吩-4-基脲,N-(1,2,3,4-四氢-4-氧代-1-萘基)酰胺和1,2,3,4-四氢-4-氧代-1-萘基脲,该过程大大提高了这些化合物的产量,并且易于扩大规模。
  • Novel 4,5,6,7-tetrahydro-7-oxy(oxy)benzo [b]thiophen-4-amine compounds
    申请人:American Cyanamid Company
    公开号:US04134899A1
    公开(公告)日:1979-01-16
    This invention relates to novel derivatives of 4,5,6,7-tetrahydro-7-oxo(oxy)benzo[b]thiophen-4-amine which are useful as animal growth regulants, and a process for the preparation thereof. The above-identified compounds of this invention are also useful as intermediates for the preparation of 4,5,6,7-tetrahydro-7-oxo(oxy)benzo[b]thien-4-ylurea compounds.
    本发明涉及4,5,6,7-四氢-7-氧(氧)苯并[b]噻吩-4-胺的新衍生物,其可用作动物生长调节剂,并提供其制备方法。本发明中所述的上述化合物也可用作制备4,5,6,7-四氢-7-氧(氧)苯并[b]噻吩-4-基脲化合物的中间体。
  • Process for oxidation of 4-amidotetrahydrobenzo [b]-thiophenes to 7-keto
    申请人:American Cyanamid Company
    公开号:US04199510A1
    公开(公告)日:1980-04-22
    There is provided a process for the preparation of an amido or an ureido derivative of certain 4,5,6,7-tetrahydro-7-oxobenzo[b]thiophenes or certain 1,2,3,4-tetrahydro-4-oxonaphthalenes which can be employed as an animal growth regulant. The process comprises: oxidizing in the presence of a cobaltic carboxylate reactant and in the absence or presence of air, a compound having the formula: ##STR1## wherein R.sub.1 and R.sub.2 are each a substituent selected from the group consisting of alkanoyl C.sub.1 -C.sub.7, halogen-substituted alkanoyl C.sub.1 -C.sub.7, carboalkoxy C.sub.1 -C.sub.4, ##STR2## and ##STR3## R.sub.3 is selected from the group consisting of hydrogen and alkyl C.sub.1 -C.sub.4 ; R.sub.4 is selected from the group consisting of hydrogen, alkyl C.sub.1 -C.sub.8, alkanoyl C.sub.2 -C.sub.4, halogen-substituted alkanoyl (C.sub.2 -C.sub.4), and ##STR4## and when the ##STR5## moiety is cyclized each represents a moiety selected from the group consisting of succinimido, maleimido and phthalimido; X and Y are each a radical selected from the group consisting of hydrogen, fluorine, chlorine, bromine, iodine, nitro, alkyl C.sub.1 -C.sub.4 ; the racemic mixtures and the optical isomers thereof.
    提供了一种制备某些4,5,6,7-四氢-7-氧代苯并[b]噻吩或某些1,2,3,4-四氢-4-氧代萘的酰胺或脲衍生物的方法,可用作动物生长调节剂。该方法包括:在钴羧酸盐反应物的存在下,在空气存在或不存在的情况下,氧化具有以下式子的化合物:##STR1##其中R.sub.1和R.sub.2均为选自羰基C.sub.1-C.sub.7,卤代羰基C.sub.1-C.sub.7,羧基烷氧基C.sub.1-C.sub.4,##STR2##和##STR3##的取代基;R.sub.3选自氢和烷基C.sub.1-C.sub.4;R.sub.4选自氢,烷基C.sub.1-C.sub.8,羰基烷C.sub.2-C.sub.4,卤代羰基(C.sub.2-C.sub.4)和##STR4##当##STR5##基团环化时,每个表示选自琥珀酰亚胺基,马来酰亚胺基和邻苯二甲酰亚胺基的基团;X和Y分别为选自氢,氟,氯,溴,碘,硝基,烷基C.sub.1-C.sub.4的基团;其外消旋混合物和其光学异构体。
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