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5-methyl-hexanoic acid tert-butyl ester | 32400-24-1

中文名称
——
中文别名
——
英文名称
5-methyl-hexanoic acid tert-butyl ester
英文别名
5-Methyl-hexansaeure-tert-butylester;Tert-butyl 5-methylhexanoate
5-methyl-hexanoic acid <i>tert</i>-butyl ester化学式
CAS
32400-24-1
化学式
C11H22O2
mdl
——
分子量
186.294
InChiKey
GLSXCGDZDSMXJX-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:
    81-84 °C(Press: 13 Torr)
  • 密度:
    0.870±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Condensation of t-Butyl Esters with Organic Halides in the Presence of Alkali Amides
    摘要:
    DOI:
    10.1021/ja01530a066
  • 作为产物:
    描述:
    醋酸叔丁酯异戊醇 在 bis(1,5-cyclooctadiene)diiridium(I) dichloride 、 potassium tert-butylate三苯基膦 作用下, 以 叔丁醇 为溶剂, 反应 15.0h, 以71%的产率得到5-methyl-hexanoic acid tert-butyl ester
    参考文献:
    名称:
    Iuchi, Yosuke; Obora, Yasushi; Ishii, Yasutaka, Journal of the American Chemical Society, 2010, vol. 132, p. 2536 - 2537
    摘要:
    DOI:
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文献信息

  • PRO-SUBSTRATES FOR LIVE CELL APPLICATIONS
    申请人:PROMEGA CORPORATION
    公开号:US20150212078A1
    公开(公告)日:2015-07-30
    Provided are pro-substrates useful in assays of living cells. The pro-substrates can be used to detect the presence or absence of enzymes, such as luciferase, in living cells. The pro-substrates can be coelenterazine derivatives or analogues.
    提供了在活细胞测定中有用的前体底物。这些前体底物可用于检测活细胞中酶的存在或缺失,如荧光素酶。这些前体底物可以是海葵素衍生物或类似物。
  • AMINOTHIAZOLE DERIVATIVE
    申请人:Yabuuchi Tetsuya
    公开号:US20120220767A1
    公开(公告)日:2012-08-30
    A compound represented by formula (1) or a pharmaceutically acceptable salt thereof, which has a PI3 kinase γ inhibitory effect and is useful as a prophylactic or therapeutic agent for articular rheumatism, Crohn's disease, irritable colitis, Sjoegren's syndrome, multiple sclerosis, systemic lupus erythematosus, asthma, atopic dermatitis, arteriosclerosis, organ transplant rejection, cancer, retinopathy, psoriasis, arthrosis deformans, age-related macular degeneration, type II diabetes, insulin resistance, obesity, non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), hyperlipemia, etc.
    由式(1)表示的化合物或其药学上可接受的盐,具有PI3激酶γ抑制作用,可用作关节风湿、克罗恩病、肠易激综合征、干燥综合征、多发性硬化、系统性红斑狼疮、哮喘、特应性皮炎、动脉硬化、器官移植排斥、癌症、视网膜病变、牛皮癣、关节病变、年龄相关性黄斑变性、2型糖尿病、胰岛素抵抗、肥胖、非酒精性脂肪肝病(NAFLD)、非酒精性脂肪性肝炎(NASH)、高脂血症等疾病的预防或治疗剂。
  • Novel peptides as NS3-serine protease inhibitors of hepatitis C virus
    申请人:Saksena K. Anil
    公开号:US20070032433A1
    公开(公告)日:2007-02-08
    The present invention discloses novel compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such compounds as well as methods of using them to treat disorders associated with the HCV protease.
    本发明揭示了具有HCV蛋白酶抑制活性的新化合物,以及制备这些化合物的方法。在另一种实施方式中,本发明揭示了包含这些化合物的药物组合物,以及使用它们治疗与HCV蛋白酶相关的疾病的方法。
  • NOVEL PEPTIDES AS NS3-SERINE PROTEASE INHIBITORS OF HEPATITIS C VIRUS
    申请人:Saksena Anil K.
    公开号:US20110117057A1
    公开(公告)日:2011-05-19
    The present invention discloses novel compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such compounds as well as methods of using them to treat disorders associated with the HCV protease.
    本发明披露了具有HCV蛋白酶抑制活性的新化合物,以及制备这些化合物的方法。在另一种实施方式中,本发明披露了包含这些化合物的制药组合物,以及使用它们治疗与HCV蛋白酶相关的疾病的方法。
  • BENZIMIDAZOLE RESPIRATORY SYNCYTIAL VIRUS INHIBITORS
    申请人:Cooymans Ludwig Paul
    公开号:US20130267508A1
    公开(公告)日:2013-10-10
    Benzimidazoles having inhibitory activity on RSV replication and having the formula the prodrugs, N-oxides, addition salts, quaternary amines, metal complexes and stereochemically isomeric forms thereof, compositions containing these compounds as active ingredient and processes for preparing these compounds and compositions.
    若干苯并咪唑化合物具有抑制RSV复制的活性,其化学式为,其前药、N-氧化物、加合盐、季铵盐、金属配合物及其立体化学异构体形式,含有这些化合物作为活性成分的组合物以及制备这些化合物和组合物的方法。
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