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2,4-dimethylpentanal | 27944-79-2

中文名称
——
中文别名
——
英文名称
2,4-dimethylpentanal
英文别名
2,4-dimethyl pentanone
2,4-dimethylpentanal化学式
CAS
27944-79-2
化学式
C7H14O
mdl
MFCD00798593
分子量
114.188
InChiKey
GPTMCJMLSOIYGU-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

  • 熔点:
    -43.35°C (estimate)
  • 沸点:
    143.73°C (estimate)
  • 密度:
    0.8225 (estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.857
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:68d97047d077048095ef99fd6cef1c29
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反应信息

  • 作为反应物:
    描述:
    2,4-dimethylpentanal 在 2.) oxidation 作用下, 以 为溶剂, 反应 6.0h, 生成
    参考文献:
    名称:
    α、β-炔酮对 II 型双自由基的新型环化
    摘要:
    环化 photochimique de mesityl-1 二甲基-4,4 pentyne-2one-1 et de «o»-tolyl-1 butyne-2one-1
    DOI:
    10.1021/ja00288a051
  • 作为产物:
    描述:
    1-ethoxy-2,4-dimethyl-pentan-2-ol 在 甲酸 作用下, 生成 2,4-dimethylpentanal
    参考文献:
    名称:
    Normant; Crisan, Bulletin de la Societe Chimique de France, 1959, p. 463
    摘要:
    DOI:
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文献信息

  • PRODUCTION METHOD FOR 4,4'-BIS(ALKYLAMINO) DIPHENYLAMINE
    申请人:Kim Jin Eok
    公开号:US20120197044A1
    公开(公告)日:2012-08-02
    The present invention relates to a production method for 4,4′-bis(alkylamino)diphenylamine, and more specifically relates to a method in which 4,4′-dinitrodiphenylamine (4,4′-DNDPA) is produced by reacting urea with nitrobenzene in the presence of a polar organic solvent and a base catalyst, and then the 4,4′-bis(alkylamino)diphenylamine (4,4′-BAADA) is produced by subjecting the 4,4′-DNDPA and a ketone to hydrogenation in the presence of a hydrogenation catalyst.
    本发明涉及一种4,4′-双(烷基氨基)二苯胺的生产方法,更具体地涉及一种方法,其中通过在极性有机溶剂和碱催化剂的存在下,使尿素与硝基苯反应来制备4,4′-二硝基二苯胺(4,4′-DNDPA),然后通过在氢化催化剂的存在下,使4,4′-DNDPA与酮进行氢化反应来制备4,4′-双(烷基氨基)二苯胺(4,4′-BAADA)。
  • Processes for preparing beta-hydroxy-ketones and alpha,beta-unsaturated ketones
    申请人:Barnicki Donald Scott
    公开号:US20050004401A1
    公开(公告)日:2005-01-06
    Processes for producing β-hydroxy-ketones and α,β-unsaturated ketones are disclosed which comprise the crossed condensation of an aldehyde with a ketone in the presence of a hydroxide or alkoxide of alkali metal or an alkaline earth metal as catalyst. The products of the process, β-hydroxy-ketones and α,β-unsaturated ketones, are useful for the preparation of many commercially important products in the chemical process industries including solvents, drug intermediates, flavors and fragrances, other specialty chemical intermediates.
    披露了生产β-羟基酮和α,β-不饱和酮的过程,这些过程包括在碱金属或碱土金属的氢氧化物或醇盐的催化下,醛与酮的交叉缩合。该过程的产品,即β-羟基酮和α,β-不饱和酮,对于化学工艺工业中许多商业上重要产品的制备非常有用,包括溶剂、药物中间体、香精和香料、以及其他专用化学品中间体。
  • CARBOXYLIC ACID DERIVATIVES AND ADHESION MOLECULE INHIBITORS CONTAINING THE SAME AS THE ACTIVE INGREDIENT
    申请人:TORAY INDUSTRIES, INC.
    公开号:EP1209147A1
    公开(公告)日:2002-05-29
    Prevention or therapy of inflammatory diseases caused by invasion of leukocytes such as monocytes, lymphocytes and eosinophils, by providing a substance which inhibits cell adhesion via an adhesion molecule, especially adhesion molecule VLA-4, is disclosed. A group of carboxylic acid derivatives represented by, for example, and adhesion molecule inhibitors comprising the same as an effective ingredient were provided.
    通过提供一种通过粘附分子抑制细胞粘附的物质,特别是粘附分子VLA-4,来预防或治疗由单核细胞、淋巴细胞和嗜酸性粒细胞侵袭引起的炎症性疾病的方法被揭示。提供了一组由羧酸衍生物代表的粘附分子抑制剂,例如,以其为有效成分的粘附分子抑制剂。
  • 1,2-Di(cyclic)substituted benzene compounds
    申请人:Kawahara Tetsuya
    公开号:US20050261291A1
    公开(公告)日:2005-11-24
    In one aspect, the present invention provides compounds having formula (1) or (100), a salt thereof or a hydrate of the foregoing, which compounds exhibit excellent cell adhesion inhibitory action or cell infiltration inhibitory action, and are useful as therapeutic or prophylactic agents for various inflammatory diseases and autoimmune diseases associated with adhesion and infiltration of leukocytes, such as inflammatory bowel disease (particularly ulcerative colitis or Crohn's disease), irritable bowel syndrome; rheumatoid arthritis, psoriasis, multiple sclerosis, asthma and atopic dermatitis. wherein R10 represents optionally substituted cycloalkyl, etc., R20-23 represent hydrogen, alkyl, alkoxy, etc., R30-32 represent hydrogen, alkyl, oxo, etc., and R40 represents optionally substituted alkyl, etc.
    在一个方面,本发明提供具有式(1)或(100)的化合物,其盐或前述的水合物,这些化合物表现出优异的细胞粘附抑制作用或细胞浸润抑制作用,并且可用作治疗或预防与白细胞粘附和浸润相关的各种炎症性疾病和自身免疫疾病的药物,例如炎症性肠病(尤其是溃疡性结肠炎或克罗恩病)、肠易激综合征;类风湿性关节炎、牛皮癣、多发性硬化、哮喘和特应性皮炎。 其中R10代表可选择地取代的环烷基等,R20-23代表氢、烷基、烷氧基等,R30-32代表氢、烷基、氧代基等,R40代表可选择地取代的烷基等。
  • 2,3,4,9-Tetrahydro-1H-carbazoles
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:EP1975159A1
    公开(公告)日:2008-10-01
    The present invention relates to 2,3,4,9-tetrahydro-1 H-carbazoles of the general formula I, in which Q, X, W, R1, R2, R3, R4 and R5 have the meaning as defined in the description. The compounds according to the invention are effective FSH antagonists and can be used for example for fertility control in men or in women, or for the prevention and/or treatment of osteoporosis.
    本发明涉及通式I的2,3,4,9-四氢-1H-咔唑, 其中Q、X、W、R1、R2、R3、R4和R5的含义如描述中所定义。 根据本发明的化合物是有效的FSH拮抗剂,可用于男性或女性的生育控制,或用于骨质疏松症的预防和/或治疗。
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