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thiepan-4-one | 22072-22-6

中文名称
——
中文别名
——
英文名称
thiepan-4-one
英文别名
Thiepan-4-on;4-thiepanone
thiepan-4-one化学式
CAS
22072-22-6
化学式
C6H10OS
mdl
——
分子量
130.211
InChiKey
FQCDOWQBRJYXCP-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:
    72-75 °C(Press: 1.5 Torr)
  • 密度:
    1.1351 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    0.7
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:8772a564cfdaee1fac04a7b2822b6e9d
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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

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文献信息

  • AZEPANE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS
    申请人:Novira Therapeutics, Inc.
    公开号:US20150197493A1
    公开(公告)日:2015-07-16
    Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.
    本文提供了一些用于治疗HBV感染的化合物,以及其药物组合物和抑制、抑制或预防受试者HBV感染的方法。
  • [EN] HISTONE METHYLTRANSFERASE INHIBITORS<br/>[FR] INHIBITEURS D'HISTONE MÉTHYLTRANSFÉRASE
    申请人:GLOBAL BLOOD THERAPEUTICS INC
    公开号:WO2017142947A1
    公开(公告)日:2017-08-24
    The present disclosure provides certain compounds of formula (I) that are histone methyltransferases G9a and/or GLP inhibitors and are therefore useful for the treatment of diseases treatable by inhibition of G9a and/or GLP such as cancers and hemoglobinpathies such as beta-thalassemia and sickle cell disease. Also provided are pharmaceutical compositions containing such compounds as well as processes and intermediates for preparing such compounds.
    本公开提供了某些公式(I)的化合物,这些化合物是组蛋白甲基转移酶G9a和/或GLP的抑制剂,因此可用于治疗可通过抑制G9a和/或GLP治疗的疾病,如癌症和血红蛋白病,例如β-地中海贫血和镰状细胞病。还提供了含有这些化合物的药物组合物以及制备这些化合物的过程和中间体。
  • [EN] A SOLVENT DRYING COMPOSITION AND PROCESSES THERFOR<br/>[FR] COMPOSITION DE SÉCHAGE PAR SOLVANT ET PROCESSUS ASSOCIÉS
    申请人:AQUAFORTUS TECH LIMITED
    公开号:WO2020204733A1
    公开(公告)日:2020-10-08
    The present disclosure relates to a solvent drying composition and processes therefor. The present disclosure more specifically relates to a solvent drying composition that in use releases water from a solvent mixture. The present disclosure also relates to a process for recovering a solvent drying composition, more specifically to a process for recovering a solvent drying composition used in an osmotic process.
    本公开涉及溶剂干燥组合物及其处理过程。具体而言,本公开涉及一种在使用中从溶剂混合物中释放水的溶剂干燥组合物。本公开还涉及一种用于回收溶剂干燥组合物的过程,更具体地说是用于回收在渗透过程中使用的溶剂干燥组合物的过程。
  • [EN] SUBSTITUTED PHENYLOXAZOLIDINONES FOR ANTIMICROBIAL THERAPY<br/>[FR] PHENYL-OXAZOLIDINONES SUBSTITUÉES POUR LA THÉRAPIE ANTIMICROBIENNE
    申请人:THE GLOBAL ALLIANCE FOR TB DRUG DEV INC
    公开号:WO2017015106A1
    公开(公告)日:2017-01-26
    The present invention relates to novel oxazolidinones (Formula I): or a pharmaceutically acceptable salt having ring A characterized by N-containing monocyclic, bicyclic or spirocyclic substituents, to their preparation, and to their use as drugs for treating Mycobacterium tuberculosis and other microbial infections, either alone or in combination with other anti-infective treatments.
    本发明涉及新型噁唑烷酮(化学式I):或具有由含氮的单环、双环或螺环取代基特征的环A的药用盐,以及其制备方法,以及作为用于治疗结核分枝杆菌和其他微生物感染的药物的用途,可以单独使用或与其他抗感染治疗结合使用。
  • SALT, ACID GENERATOR, RESIST COMPOSITION AND METHOD FOR PRODUCING RESIST PATTERN
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:US20210371376A1
    公开(公告)日:2021-12-02
    A salt represented by formula (I): wherein R 1 and R 2 each independently represent a hydroxy group, —O—R 10 , —O—CO—O—R 10 or —O-L 1 -CO—O—R 10 ; L 1 represents an alkanediyl group having 1 to 6 carbon atoms; R 4 , R 5 , R 7 and R 8 each independently represent a halogen atom, an alkyl fluoride group having 1 to 12 carbon atoms or a hydrocarbon group having 1 to 18 carbon atoms, the hydrocarbon group may have a substituent, and —CH 2 — included in the hydrocarbon group may be replaced by —O—, —CO—, —S— or —SO 2 —; R 10 represents an acid-labile group; X 1 and X 2 each independently represent an oxygen atom or a sulfur atom; m1 represents an integer of 1 to 5, m2 and m8 represent an integer of 0 to 5, m4, m5 and m7 represent an integer of 0 to 4; and AI − represents an organic anion.
    一种由化学式(I)表示的盐:其中R1和R2分别代表一个羟基,-O-R10,-O-CO-O-R10或-O-L1-CO-O-R10;L1代表具有1至6个碳原子的烷二基基团;R4、R5、R7和R8分别独立地表示卤素原子,具有1至12个碳原子的烷基氟基团或具有1至18个碳原子的碳氢基团,碳氢基团可能有取代基,并且碳氢基团中包含的-CH2-可被-O-,-CO-,-S-或-SO2-取代;R10代表一个酸敏感基团;X1和X2分别独立地表示一个氧原子或一个硫原子;m1表示1至5的整数,m2和m8表示0至5的整数,m4、m5和m7表示0至4的整数;AI-代表一个有机阴离子。
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同类化合物

硫杂环庚烷-2-酮 硫杂环庚烷 环己硫醚 桉叶硫醚 四氢-6-硫代-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3-酮 二氢-7-丁基-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 二氢-1,4-二甲基-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 二氢-1,4-乙基桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 β.-D-半乳吡喃糖,1,6-二脱氧-1,6-环硫- 6-硫杂双环[3.2.1]辛烷 6-甲基-7-硫杂二环[4.1.0]庚烷 5-氧代噻吩-3-羧酸甲酯 5-氧代-4-噻吩甲酸乙酯 4,7,7-三甲基-6-硫代二环[3.2.1]辛烷 3-硫杂二环[3.2.1]辛烷-2-酮,1,8,8-三甲基-,(1R)- 3-甲基噻吩1,1-二氧化物 2-羟基噻烷 1-癸基2-[[1-(2-氯-5-磺基苯基)-4,5-二氢-3-甲基-5-羰基-1H-吡唑-4-基]偶氮]苯酸酯 1,6:4,5-二去氢-2,3-二脱氧-1-硫代己糖醇 (1S,4S,5S)-4,7,7-三甲基-6-硫代二环[3.2.4]辛烷 4-Acetoxy-5-chloro-3,3,6,6-tetramethylthiacycloheptane 3-phenylthiepan-3-ol 4-isopropenyl-1-methyl-7-thiabicyclo[4.1.0]heptane 8,9,10,11-tetrachloro-4-thiatricyclo<5.4.0.02,6>undeca-8,10-diene 4,4-dioxide cis-bicyclo<3.2.01,5>-3-thiepane-2,4-dione 1-phenyl-2,2,3,3-tetracyano-7,8-dithiabicyclo<3.2.1>octane 2-Thiabicyclo[3.2.2]non-5-en-3-one oxime 2-Thiabicyclo[3.2.2]nonan-3-one oxime 1,6-dideoxy-1,6-epithio-β-D-glucopyranose S,S-dioxide (3aS,4R,8S,8aR)-2,2-dimethylhexahydrothiepino[4,5-d][1,3]dioxole-4,8-diol (3aS,4R,8R,8aS)-2,2-Dimethyl-hexahydro-thiepino[4,5-d][1,3]dioxole-4,8-diol 2,2-dimethylhexahydrothiepino[4,5-d][1,3]dioxole-4,8-diol (1S,4R,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one 3,7-dithia(3.3.2)propellane-3,3,7,7-tetroxide 1-Methyl-4-(2-methylthiiran-2-yl)-7-thiabicyclo[4.1.0]heptane 3-Vinylcyclohexen-diepisulfid 7-tert-Butyl-4-methyl-8-oxa-3-thia-7-azabicyclo<4.2.1>nonan 9-Thiabicyclo[4.2.1]non-7-ene 9-Thiabicyclo[4.2.1]nonane 4-Thiahomoadamantane 4,4-Dioxide 4-Thiahomoadamantane 4-Thiahomoadamantan-2-one ethyl thiacyclohepten-4-one-3-carboxylate 1,1-dioxide 1-Morpholino-6-thia-bicyclo<3.2.0>heptan-S-dioxid 1,6-Bis-dec-9-enyl-9-thia-bicyclo[4.2.1]nonane 9,9-dioxide 4-methylthiepane 1,1-dioxide (S)-(1,1-dioxothiepan-4-yl)methanol (1,1-dioxothiepan-4-yl)methanol 3-thia-bicyclo[3.2.1]octane 1,6-Anhydo-1(6)-thio-L-idit