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5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-4-one | 61942-70-9

中文名称
——
中文别名
——
英文名称
5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-4-one
英文别名
5,6,7,8-tetrahydrocyclohepta[b]thiophen-4-one
5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-4-one化学式
CAS
61942-70-9
化学式
C9H10OS
mdl
——
分子量
166.244
InChiKey
VJXXPASWWIYOEK-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:
    156 °C(Press: 13 Torr)
  • 密度:
    1.187±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    45.3
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:bbf9662a1c4d9e434859dd3c09a650cb
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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

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文献信息

  • Substituted tetrahydrobenzothiophenes and method of preparation thereof
    申请人:American Cyanamid Company
    公开号:US04150035A1
    公开(公告)日:1979-04-17
    This disclosure describes novel 5,6,7,8-tetrahydro-4H-cyclohepta[b]thiophen-4-amines useful as intermediates for the preparation of animal growth regulants.
    这份披露描述了作为动物生长调节剂制备中间体有用的新型5,6,7,8-四氢-4H-环庚[b]噻吩-4-胺。
  • 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硫脲,以提高饲料效率并加快生长速度。
  • Generation of cycloheptynes and cyclooctynes via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates
    作者:Suguru Yoshida、Fumika Karaki、Keisuke Uchida、Takamitsu Hosoya
    DOI:10.1039/c5cc01784j
    日期:——

    Cycloheptynes and cyclooctynes have been efficiently generated via a sulfoxide–magnesium exchange reaction of readily synthesized 2-sulfinylcycloalkenyl triflates.

    环庚烯和环庚炔已通过易于合成的2-磺酰基环烯基三氟甲磺酸酯的亚砜-交换反应高效生成。
  • [EN] HETEROARYL-FUSED MACROCYCLIC PYRIMIDINE DERIVATIVES<br/>[FR] DÉRIVÉS MACROCYCLIQUES DE PYRIMIDINE À GROUPE HÉTÉROARYLE CONDENSÉ
    申请人:ABBOTT LAB
    公开号:WO2009137492A1
    公开(公告)日:2009-11-12
    Heteroaryl-fused macrocyclic 2,4-diaminopyrimidine compounds of formula (I) wherein W, G1, G2, A1 and R1 are defined in the description, compositions comprising such compounds, methods for making the compounds, and methods of treating and preventing the progression of diseases, conditions, and disorders using such compounds and compositions are described herein.
    Heteroaryl-融合的大环2,4-二氨基嘧啶化合物的化学式(I),其中W、G1、G2、A1和R1在描述中有定义,本文描述了包含这些化合物的组合物,制备这些化合物的方法,以及使用这些化合物和组合物治疗和预防疾病、症状和疾病进展的方法。
  • Polycyclic heteroaromatic ring construction driven by silver/cobalt co-catalyzed desulfonylative and defluorinative fragment-recombination of enol nonaflates with amidines
    作者:Ting Xie、Yao-Wei Zhang、Li-Li Liu、Zhi-Liang Shen、Teck-Peng Loh、Xue-Qiang Chu
    DOI:10.1039/c8cc07409g
    日期:——

    A novel Ag(i)/Co(ii) co-catalyzed tandem fragmentation and recombination reaction commencing from detachable nonaflates and amidines has been developed.

    一个新颖的Ag(I)/Co(II)共催化的串联裂解和重组反应,从可分离的Nonaflates和Amidines开始。
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酮替芬EP杂质A 酮替芬 苯噻啶苹果酸盐 苯噻啶盐酸盐 苯噻啶 益托洛替芬 富马酸酮替芬 去甲酮替芬富马酸氢盐 乙基2-[(乙基氨基甲硫杂酰)氨基]-5,6,7,8-四氢-4H-环庚三烯并[b]噻吩-3-羧酸酯 [2,3-d]噻吩并环庚三烯酮 9-氧代酮替芬 9,10-二溴-9,10-二氢-4H-苯并[4,5]环庚并[1,2-b]噻吩-4-酮 9,10-二氧代酮替芬 9, 10-二氢-4H-苯并[4, 5]环庚三烯[1, 2-b]噻吩-4-酮 6H-环庚三烯并[c]噻吩-6-酮,1,3,5,7-四甲基- 5,6,7,8-四氢-4h-环庚基[b]噻吩-2-羧酸 5,6,7,8-四氢-4H-环庚[b]噻吩-2-羧酸酰肼 4H-环庚三烯并[b]噻吩-3-羧酸,5,6,7,8-四氢-2-[3-(羟甲基)-5-甲基-4H-1,2,4-三唑-4-基]-,甲基酯 4-羟基酮替芬 4-(哌啶-4-亚基)-4H-苯并[4,5]环庚三烯并[1,2-B]噻吩-10(9H)-酮 4-(3'-甲基氨基丙基亚基)-9,10-二氢-4H-苯并(4,5)环庚并(1,2-b)噻吩 4,9-二氢-4-(1-甲基-4-哌啶基亚基)-10H-苯并[4,5]环庚三烯并[1,2-b]噻吩-10-酮 N-氧化物; 酮替芬 N-氧化物 2-溴-9,10-二氢-4H-苯并(4,5)环庚并(1,2-b)噻吩-4-酮 2-氯-N-(3-氰基-5,6,7,8-四氢-4H-环戊并[b]噻吩-2-基)-乙酰胺 2-氨基环庚烷并[B]噻吩-3-羧酸乙酯 2-氨基-N-甲基-5,6,7,8-四氢-4H-环庚并[b]噻吩-3-甲酰胺 2-氨基-N-乙基-5,6,7,8-四氢-4H-环庚并[b]噻吩-3-甲酰胺 2-氨基-5,6,7,8-四氢-4H-环庚基[b]噻吩-3-羧酰胺 2-氨基-5,6,7,8-四氢-4H-环庚基[b]噻吩-3-甲腈 2-氨基-5,6,7,8-四氢-4H-环庚[B]噻吩-3-甲酸甲酯 2-乙酰氨基-5,6,7,8-四氢-4H-环庚并[b]噻吩-3-羧酸 2-[(3-氯-1-氧代丙基)氨基]-5,6,7,8-四氢-4H-环庚并[b]噻吩-3-羧酸乙酯 2-(2-氯乙酰基氨基)-5,6,7,8-四氢-4H-环庚[b]噻吩-3-羧酸乙酯 10-甲氧基-4H-苯并[4,5]环庚三烯并[1,2-b]噻吩-4-酮 10-甲氧基-4-(1-甲基-4-哌啶基)-4H-苯并[4,5]环庚三烯并[1,2-B]噻吩-4-醇 1,3-二氢-1-[1-[(5,6,7,8-四氢-4H-环庚[b]噻吩-2-基)羰基]-4-哌啶基]-2H-苯并咪唑-2-酮 (3E)-3-(9,10-二氢-4H-苯并[4,5]环庚三烯并[1,2-b]噻吩-4-亚基)-N,N-二甲基丙烷-1-胺 (+/-)-10-<3-Dimethylamino-propyl>-4,5-dihydro-10H-benzo<5,6>cyclohepta<1,2-b>thiophen-10-ol methyl 2-[3-(acetylamino)-6-methyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophen-6-yl]acetate 10-<3-Dimethylamino-propyliden>-4,5-dihydro-10H-benzo<5,6>-cyclohepta<1,2-b>thiophen ethyl 3-[4-(1-methylpiperidin-4-ylidene)-10-oxo-9,10-dihydro-4H-1-thiabenzo[f]azulen-2-yl]acrylate 2-t-butoxycarbonylamino-4-(1-methylpiperidin-4-ylidene)-9,10-dihydro-4H-1-thiabenzo[f]azulene ethyl 4-[1-(2-ethoxyethyl)piperidin-4-ylidene]-9,10-dihydro-4H-1-thiabenzo[f]azulene-2-carboxylate hydrochloride Ethyl 4-(1-propylpiperidin-4-ylidene)-9,10-dihydro-4H-1-thiabenzo[f]azulene-2-carboxylate hydrochloride 4-(6-chloro-2-methyl-benzo[4,5]cyclohepta[1,2-b]thiophen-4-ylidene)-1-methyl-piperidine methyl 2-[2-(acetylamino)-6-methyl-7-oxo-4,5,6,7-tetrahydrobenzo[b]thiophen-6-yl]acetate 2-ureidomethyl-4-(1-methylpiperidin-4-ylidene)-9,10-dihydro-4H-1-thiabenzo[f]azulene 2-[2-(9,10-dihydro-benzo[4,5]cyclohepta[1,2-b]thiophen-4-ylidene)-ethyl]-piperidine-1-carboxylic acid ethyl ester 4-[1-(2-ethoxyethyl)piperidin-4-ylidene]-9,10-dihydro-4H-1-thiabenzo[f]azulene-2-carboxylic acid