5-丙基-1,3-环己烷二酮 | 57641-89-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 5-丙基-1,3-环己烷二酮
• 英文名称: 5-propylcyclohexane-1,3-dione
• CAS: 57641-89-1
• 化学式: C₉H₁₄O₂
• mdl: MFCD00129456
• 分子量: 154.209
• InChiKey: RHELOIKNLIFWEO-UHFFFAOYSA-N

物化性质

• 熔点：
  95-99 °C
• 沸点：
  267.1±23.0 °C(Predicted)
• 密度：
  1.004±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.777
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2914299000
• 储存条件：
  室温

反应信息

• 作为反应物：
  描述：

  5-丙基-1,3-环己烷二酮 在 氯磺酸 作用下， 以 1,4-二氧六环 、 乙醇 为溶剂， 反应 34.5h， 生成 3-bromo-5-(3-cyano-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinolin-4-yl)-2-hydroxy-N,N-dimethyl-benzenesulfonamide
  参考文献：
  名称：

  WO2006/117370

  摘要：

  公开号：
• 作为产物：
  描述：

  (4E)-4-庚烯-2-酮 在 乙醇 、 氢溴酸 、 溶剂黄146 作用下， 生成 5-丙基-1,3-环己烷二酮
  参考文献：
  名称：

  Pathogenicity of fungi isolated from Quercus suber in Catalonia (NE Spain)

  摘要：

  Summary Thirty‐four fungal species isolated from cork oak (Quercus suber) in Catalonia (NE Spain) during 1992–95 were tested for pathogenicity either in stem, leaf or root inoculations. Eleven species were found to be pathogenic on stem: Biscogniauxia mediterranea, Botryosphaeria stevensii, Diatrype cf. stigma, Endothia gyrosa, Fusarium solani, Graphium sp., Ophiostoma quercus, Phomopsis sp., Phytophthora cinnamomi, Sporendocladia bactrospora and an unidentified Coelomycete. Three fungi showed pathogenic effects on leaves: Dendrophoma myriadea, Lembosia quercina and Phomopsis quercella. No clear pathogenic effects were detected in the root inoculation experiment. Trunk pathogens were differentiated into two groups according to the effects induced in the inoculated plants; B. stevensii, Phomopsis sp. and P. cinnamomi caused the death of the inoculated plants and induced the formation of large cankers and vascular necroses. The other pathogenic species also produced severe cankers and vascular lesions, but no significant mortality was detected. Water stress increased the lesions caused by B. mediterranea and Phomopsis sp., but limited those of P. cinnamomi and the rest of the inoculated fungi. However, water stress did not significantly affect the damage caused by B. stevensii, which was the most virulent of the species tested. Leaf pathogens only showed their effects if the leaf cuticle was previously damaged. Lembosia quercina caused small dark lesions whereas D. myriadea and P. quercella produced large necrotic areas in well‐watered plants. The lesions caused by the last two fungi were reduced by water stress.

  DOI：

  10.1046/j.1439-0329.2000.00208.x

文献信息

• Arylsulfonylcarbamoyl-1,3-dicarbonylacyclic compounds
  申请人：Mead Johnson & Company

  公开号：US03998879A1

  公开（公告）日：1976-12-21

  A new class of arylsulfonylcarbamoyl-1,3-cyclohexanediones and arylsulfonylcarbamoyl-1,3-dicarbonylacyclic compounds are disclosed. These substances have hypoglycemic or hyperglycemic properties and are of value in controlling abnormal blood sugar levels. The arylsulfonylcarbamoyl derivatives of 1,3-dicarbonylalicyclic and acyclic compounds are prepared by reacting an arylsulfonylisocyanate with a 1,3-dicarbonylalicyclic or acyclic reactant. Typical embodiments are 2-(N-p-chlorobenzenesulfonylcarbamoyl)-5,5-dimethylcyclohexane-1,3-dione and 5-(1-ethylpropyl)-2-(N-p-chlorobenzenesulfonylcarbamoyl)-1,3-cyclohexanedi one.

  一类新的芳基磺酰脲基-1,3-环己二酮和芳基磺酰脲基-1,3-二羰基环状化合物被公开。这些物质具有降血糖或升血糖的性质，在控制异常血糖水平方面具有价值。通过将芳基磺酰异氰酸酯与1,3-二羰基环状或非环状反应物反应，制备了1,3-二羰基环状和非环状化合物的芳基磺酰脲衍生物。典型的实施例包括2-(N-对氯苯磺酰脲基)-5,5-二甲基环己烷-1,3-二酮和5-(1-乙基丙基)-2-(N-对氯苯磺酰脲基)-1,3-环己二酮。
• Fluorescent 1-hydroxy-10-alkylacridin-9(10H)-one BF2-chelates: Large Stokes shift and long emission decay times
  作者：Andreas Russegger、Sergey M. Borisov

  DOI：10.1016/j.dyepig.2020.108816

  日期：2021.1

  New 1-hydroxy-10-alkylacridin-9(10H)-one BF2-chelates absorb in the blue-green part of the electromagnetic spectrum and emit fluorescence with moderate quantum yields of 8–45% in toluene. The dyes show large Stokes shifts about 4300 cm−1, decay times between 5 ns and 15 ns in toluene and high photostabilities. Introduction of a fluorine atom into the acridone cycle results in an increase of the fluorescence

  新的1-羟基-10-烷基ac啶9-9 （10 H）-1 BF 2螯合物在电磁光谱的蓝绿色部分吸收并发出荧光，在甲苯中的荧光量子产率为8–45％。染料在甲苯中显示出大的斯托克斯位移，约为4300 cm -1，衰减时间在5 ns到15 ns之间，并且具有高光稳定性。将氟原子引入a啶酮循环会导致荧光量子产率和衰减时间的增加，而固定在刚性聚合物基质（聚苯乙烯）中的寿命则进一步延长至18 ns。较大的斯托克斯位移和长的发射衰减时间使该染料类成为时间分辨成像和传感应用的有趣平台。
• Enamine derivatives
  申请人：——

  公开号：US20020037909A1

  公开（公告）日：2002-03-28

  Enamine derivatives of formula (1) are described: 1 wherein R 1 is a group Ar 1 L 2 Ar 2 Alk- in which Ar 1 is an aromatic or heteroaromatic group, L 2 is a covalent bond or a linker atom or group, Ar 2 is an arylene or heteroarylene group and Alk is a chain —CH 2 —CH(R)—, —CH═C(R)— or 2 in which R is a carboxylic acid or a derivative or biostere thereof; R 2 is a hydrogen atom or a C 1-6 alkyl group; Cy is a cycloaliphatic or heterocycloaliphatic ring in which X is a N atom or a C(R w ) group; R x is a oxo, thioxo, or imino group; R w and R z is each a hydrogen atom or optional substituent; provided that Cy is not a cyclobutenedione group; and the salts, solvates, hydrates and N-oxides thereof. The compounds are able to inhibit the binding of integrins to their ligands and are of use in the prophylaxis and treatment of immune or inflammatory disorders, or disorders involving the inappropriate growth or migration of cells.

  描述了公式（1）的Enamine衍生物：其中R1是Ar1L2Ar2Alk-中的一个基团，其中Ar1是芳香族或杂环芳基，L2是共价键或连接原子或基团，Ar2是芳基或杂环芳基，Alk是链—CH2—CH（R）—，—CH═C（R）—或其中R是羧酸或其衍生物或生物类似物；R2是氢原子或C1-6烷基基团；Cy是环脂环或杂环脂环，其中X是N原子或C（Rw）基团；Rx是氧化、硫代氧化或亚胺基团；Rw和Rz分别是氢原子或可选取代基；前提是Cy不是环丁二酮基团；以及它们的盐、溶剂合物、水合物和N-氧化物。这些化合物能够抑制整合素与其配体的结合，并可用于预防和治疗免疫或炎症性疾病，或涉及细胞异常生长或迁移的疾病。
• DIHYDROPYRIDINE DERIVATIVES
  申请人：Van Straten Nicole Corine Renee

  公开号：US20090215773A1

  公开（公告）日：2009-08-27

  The present invention relates to dihydropyridine derivatives having general formula (I) or a pharmaceutically acceptable salt thereof, wherein R 1 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, phenyl, (1-5C)heteroaryl R 2 , R 3 are independently (1-4C)alkyl, (2-4C)alkenyl, (2-4C)alkynyl, (1-4C)alkoxy, (24C)alkenyloxy, (2-4C)alkynyloxy, halogen X is SO 2 , CH 2 , C(O) or X is absent R 4 is (1-6C)alkyl, (2-6C)alkenyl, (2-6C)alkynyl, (3-6C)cycloalkyl, (3-6C)cycloalkenyl, (3-6C)cycloalkyl(1-4C)alkyl, (2-6C)heterocycloalkyl, (2-6C)heterocycloalkyl(14C)alkyl, (6-1 OC)aryl, (6-10C)aryl(1-4C)alkyl, (1-9C)heteroaryl or (1-9C)heteroaryl(14C)alkyl. The compounds are useful for the treatment of fertility disorders.

  本发明涉及具有通式（I）或其药学上可接受的盐的二氢吡啶衍生物，其中R1为（1-6C）烷基、（2-6C）烯基、（2-6C）炔基、苯基、（1-5C）杂环芳基，R2、R3独立地为（1-4C）烷基、（2-4C）烯基、（2-4C）炔基、（1-4C）烷氧基、（2-4C）烯氧基、（2-4C）炔氧基、卤素X为SO2、CH2、C(O)或X不存在，R4为（1-6C）烷基、（2-6C）烯基、（2-6C）炔基、（3-6C）环烷基、（3-6C）环烯基、（3-6C）环烷基（1-4C）烷基、（2-6C）杂环烷基、（2-6C）杂环烷基（1-4C）烷基、（6-10C）芳基、（6-10C）芳基（1-4C）烷基、（1-9C）杂环芳基或（1-9C）杂环芳基（1-4C）烷基。这些化合物可用于治疗生育障碍。
• 4-Phenyl-5-Oxo-1,4,5,6,7,8,- Hexahydroquinoline Derivatives as Medicaments for the Treatment of Infertility
  申请人：Timmers Cornelis Marius

  公开号：US20080300270A1

  公开（公告）日：2008-12-04

  The invention relates to a 4-phenyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline derivative according to Formula (I), wherein the substituents are defined as in the description, or a pharmaceutically salt thereof. The compounds of this invention are potent FSH receptor activators and may be used for treating fertility disorders in e.g. controlled ovarian hyperstimulation and IVF procedures.

  该发明涉及一种根据式(I)定义的4-苯基-5-酮-1,4,5,6,7,8-六氢喹啉衍生物，其中取代基如描述中所定义，或其药用盐。本发明的化合物是强效FSH受体激活剂，可用于治疗例如控制性卵巢过度刺激和体外受精程序中的生育障碍。