2-butyl-heptanoic acid | 22058-70-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2-butyl-heptanoic acid
• 英文别名: 2-Butyl-heptansaeure；2-Butyl-heptan-carbonsaeure；2-n-Butylheptansaeure；Decan-5-carbonsaeure；2-Butylheptanoic acid
• CAS: 22058-70-4
• 化学式: C₁₁H₂₂O₂
• mdl: MFCD02258979
• 分子量: 186.294
• InChiKey: UEWINXFENVHYDF-UHFFFAOYSA-N

物化性质

• 沸点：
  135 °C(Press: 3 Torr)
• 密度：
  0.893 g/cm3(Temp: 25 °C)

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  13
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.909
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-butyl-heptanoic acid 在 草酰氯 、 N,N-二甲基甲酰胺 作用下， 以 苯 为溶剂， 生成 2-Butylheptanoyl chloride
  参考文献：
  名称：

  [EN] IONIZABLE CATIONIC LIPIDS AND LIPID NANOPARTICLES, AND METHODS OF SYNTHESIS AND USE THEREOF
  [FR] NANOPARTICULES LIPIDIQUES ET LIPIDES CATIONIQUES IONISABLES, ET LEURS PROCÉDÉS DE SYNTHÈSE ET D'UTILISATION

  摘要：

  Provided are ionizable cationic lipids and lipid nanoparticles for the delivery of nucleic acids to cells (e.g., immune cells), and methods of making and using such lipids and targeted lipid nanoparticles.

  公开号：

  WO2023240156A1
• 作为产物：
  描述：

  正丁基-1-辛烯 在 臭氧 、 乙酸乙酯 作用下， 生成 2-butyl-heptanoic acid
  参考文献：
  名称：

  Ziegler et al., Justus Liebigs Annalen der Chemie, 1950, vol. 567, p. 99,114

  摘要：

  DOI：

文献信息

• [EN] DIHYDROPYRAZOLOPYRIDINE COMPOUNDS<br/>[FR] COMPOSES DE DIHYDROPYRAZOLOPYRIDINE
  申请人：MITSUBISHI PHARMA CORP

  公开号：WO2004014910A1

  公开（公告）日：2004-02-19

  The present invention provides dihydropyrazolopyridine compounds represented by the formula (I):wherein each symbol is as defined in the specification, optically active forms thereof, and pharmaceutically acceptable salts thereof and hydrates thereof. The compounds of the present invention show a selective and strong inhibitory activity on glycogen synthase kinase-3 beta (GSK-3β), and are useful as medicaments for prevention and/or treatment of diabetes, diabetic complications and neurodegenerative diseases or as immunopotentiators.

  本发明提供了由式(I)表示的二氢吡唑吡啶化合物，其中每个符号如规范中定义，其光学活性形式，以及其药学上可接受的盐和水合物。本发明的化合物显示出对糖原合成酶激酶-3β（GSK-3β）的选择性和强烈的抑制活性，并可用作预防和/或治疗糖尿病、糖尿病并发症和神经退行性疾病或免疫增强剂的药物。
• [EN] DERIVATIVES OF AZA ADAMANTANE AND USES THEREOF<br/>[FR] DÉRIVÉS D'AZA-ADAMANTANE ET LEURS UTILISATIONS
  申请人：CONNEXIOS LIFE SCIENCES PVT LTD

  公开号：WO2013111150A1

  公开（公告）日：2013-08-01

  The present invention relates to certain amide derivatives that have the ability to inhibit 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) and which are therefore useful in the treatment of certain disorders that can be prevented or treated by inhibition of this enzyme. In addition the invention relates to the compounds, methods for their preparation, pharmaceutical compositions containing the compounds and the uses of these compounds in the treatment of certain disorders. It is expected that the compounds of the invention will find application in the treatment of conditions such as non-insulin dependent type 2 diabetes mellitus (NIDDM), insulin resistance, obesity, impaired fasting glucose, impaired glucose tolerance, lipid disorders such as dyslipidemia, hypertension and as well as other diseases and conditions.

  本发明涉及某些酰胺衍生物，具有抑制11-β-羟基类固醇脱氢酶1型（11β-HSD-1）的能力，因此在预防或治疗可以通过抑制该酶而预防或治疗的某些疾病方面具有用处。此外，本发明涉及这些化合物、其制备方法、含有这些化合物的药物组合物以及这些化合物在治疗某些疾病中的用途。预计本发明的化合物将在治疗非胰岛素依赖型2型糖尿病（NIDDM）、胰岛素抵抗、肥胖、空腹血糖受损、糖耐量受损、脂质紊乱如血脂异常、高血压以及其他疾病和病症的治疗中发挥作用。
• [EN] SUBSTITUTED -1,3,8-TRIAZASPIRO[4.5]DECANE-2,4-DIONES<br/>[FR] 1,3,8-TRIAZASPIRO[4,5]DÉCANE-2,4-DIONES SUBSTITUÉES
  申请人：MERCK SHARP & DOHME

  公开号：WO2010147776A1

  公开（公告）日：2010-12-23

  The present invention relates to substituted 1,3,8-triazaspiro[4.5]decame-2,4-diones useful as HIF prolyl hydroxylase inhibitors to treat anemia and like conditions.

  本发明涉及替代的1,3,8-三氮杂螺[4.5]癸烯-2,4-二酮，可用作HIF脯氨酸羟化酶抑制剂，用于治疗贫血和类似症状。
• Dimerisation of polyacetylenic aldehydes with elimination of carbon monoxide
  作者：R. K. Bentley、U. Graf、Ewart R. H. Jones、R. A. M. Ross、V. Thaller、R. A. Vere Hodge

  DOI：10.1039/j39690000683

  日期：——

  Hexa-2,4-diynal, octa-2,4-diynal, and octa-2,4,6-triynal (R[CC]n·CHO) dimerise in concentrated solution with evolution of carbon monoxide, to give products of the type R[CC]n– 1·CHC(CHO)·[CC]nR; above 100° even phenylpropargyl aldehyde reacts analogously. Both geometrical isomers of the ‘dimers’ were detected and characterised.

  在浓溶液中随着六氧化二碳的逸出，六（2,4-二炔），八（2,4-二炔）和八（2,4,6-三炔）（R [CC ] n ·CHO）二聚，得到类型R [C C] n – 1 ·CH C（CHO）·[C C] n R；高于100°时，甚至苯基炔丙基醛也会发生类似反应。“二聚体”的两个几何异构体均被检测并表征。
• TRIFLUOROMETHYLTHIOPHENIUM DERIVATIVE SALT, METHOD FOR PRODUCING THE SAME, AND METHOD FOR PRODUCING TRIFLUOROMETHYL-CONTAINING COMPOUNDS USING THE SAME
  申请人：Shibata Norio

  公开号：US20120130090A1

  公开（公告）日：2012-05-24

  A trifluoromethylthiophenium derivative salt useful as synthetic intermediates for pharmaceuticals and agrochemicals, a method for producing the same, and a method for producing trifluoromethyl-containing compounds using the same are provided. An S-(trifluoromethyl)-benzo[b]thiophenium derivative salt is represented by the following general formula (1): wherein R 1 , R 2 , R 3 , and R 4 are each independently a hydrogen atom, a methyl group, an ethyl group, a linear, branched, or cyclic alkyl group having 3 to 10 carbon atoms, a methoxy group, an ethoxy group, a linear, branched, or cyclic alkyloxy group having 3 to 10 carbon atoms, a fluorine atom, a chlorine atom, a bromine atom, a nitro group, or a cyano group, R 5 is a methyl group, an ethyl group, a linear, branched, or cyclic alkyl group having 3 to 10 carbon atoms, a phenyl group, or a substituted phenyl group, and X − represents an anion. Various trifluoromethyl-containing compounds are produced using a method for producing the S-(trifluoromethyl)-benzo[b]thiophenium derivative salt, and using the S-(trifluoromethyl)-benzo[b]thiophenium derivative salt as a trifluoromethylating agent.

  本发明提供一种三氟甲基噻吩盐衍生物，可用作制药和农药的合成中间体，以及其制备方法和使用该盐衍生物制备含三氟甲基化合物的方法。S-(三氟甲基)-苯并[b]噻吩盐衍生物由下列普通式（1）表示：其中，R1、R2、R3和R4各自独立地是氢原子、甲基基团、乙基基团、具有3至10个碳原子的线性、支链或环烷基基团、甲氧基基团、乙氧基基团、具有3至10个碳原子的线性、支链或环烷氧基基团、氟原子、氯原子、溴原子、硝基或氰基，R5是甲基基团、乙基基团、具有3至10个碳原子的线性、支链或环烷基基团、苯基或取代苯基，X-表示阴离子。使用制备S-(三氟甲基)-苯并[b]噻吩盐衍生物的方法以及使用S-(三氟甲基)-苯并[b]噻吩盐衍生物作为三氟甲基化试剂可以制备各种三氟甲基含量的化合物。